Recent Advances in Self-assembled Nano-therapeutics
English
Recent Advances in Self-assembled Nano-therapeutics
-
-
-
[1]
Salomon J. A., Wang H., Freeman M. K.. Healthy life expectancy for 187 countries, ,1990-2010:a systematic analysis for the global burden of disease study[J]. Lancet, 2013, 381(9867): 628-628.
-
[2]
Porter R.. The nature of suffering and the goals of medicine[J]. Hist. Phil. Life Sci., 1997, 19(2): 297-298.
-
[3]
Liu Y., Li J., Lu Y.. Enzyme therapeutics for systemic detoxification[J]. Adv. Drug Deliv. Rev., 2015, 90(1): 24-39.
-
[4]
Duncan R.. Polymer conjugates as anticancer nanomedicines[J]. Nat. Rev. Cancer, 2006, 6(9): 688-701. doi: 10.1038/nrc1958
-
[5]
Farokhzad O. C., Langer R.. Impact of nanotechnology on drug delivery[J]. ACS Nano, 2009, 3(1): 16-20. doi: 10.1021/nn900002m
-
[6]
Zhang L., Gu F. X., Chan J. M., Wang A. Z.. Nanoparticles in medicine:Therapeutic applications and developments[J]. Clin. Pharmacol. Ther., 2008, 83(5): 761-769. doi: 10.1038/sj.clpt.6100400
-
[7]
Ferrari M.. Cancer nanotechnology:opportunities and challenges[J]. Nat. Rev. Cancer, 2005, 5(3): 161-171. doi: 10.1038/nrc1566
-
[8]
Singh K. K.. Nanotechnology in cancer detection and treatment[J]. Technol. Cancer Res. T., 2005, 4(6): 583-583. doi: 10.1177/153303460500400601
-
[9]
Couvreur P., Vauthier C.. Nanotechnology:intelligent design to treat complex disease[J]. Pharm. Res., 2006, 23(7): 1417-1450. doi: 10.1007/s11095-006-0284-8
-
[10]
Bertrand N., Wu J., Xu X., Kamaly N.. Cancer nanotechnology:the impact of passive and active targeting in the era of modern cancer biology[J]. Adv. Drug Deliv. Rev., 2014, 66(1): 2-25.
-
[11]
Ozin G. A., Hou K., Lotsch B. V., Cademartiri L.. Nanofabrication by self-assembly[J]. Mater. Today, 2009, 12(5): 12-23. doi: 10.1016/S1369-7021(09)70156-7
-
[12]
Mastrangeli M., Abbasi S., Varel C., Van Hoof C.. Self-assembly from milli-to nanoscales:methods and applications[J]. J. Micromech Microeng., 2009, 19(8): . doi: 10.1088/0960-1317/19/8/083001
-
[13]
Bishop K. J., Wilmer C. E., Soh S., Grzybowski B. A.. Nanoscale forces and their uses in self-assembly[J]. Small, 2009, 5(14): 1600-1630. doi: 10.1002/smll.v5:14
-
[14]
Peer D., Karp J. M., Hong S., FaroKhzad O. C.. Nanocarriers as an emerging platform for cancer therapy[J]. Nat. Nanotechnol., 2007, 2(12): 751-760. doi: 10.1038/nnano.2007.387
-
[15]
Letchford K., Burt H.. A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures:micelles, nanospheres, nanocapsules and polymersomes[J]. Eur. J. Pharm. Biopharm., 2007, 65(3): 259-269. doi: 10.1016/j.ejpb.2006.11.009
-
[16]
Chandler D.. Interfaces and the driving force of hydrophobic assembly[J]. Nature, 2005, 437(7059): 640-647. doi: 10.1038/nature04162
-
[17]
Wang C., Wang Z., Zhang X.. Amphiphilic building blocks for self-assembly:From amphiphiles to supra-amphiphiles[J]. Acc. Chem. Res., 2012, 45(4): 608-618. doi: 10.1021/ar200226d
-
[18]
Hill J. P., Shrestha L. K., Ishihara S., Ji Q.. Self-assembly:from amphiphiles to chromophores and beyond[J]. Molecules, 2014, 19(6): 8589-8609.
-
[19]
Rösler A., Vandermeulen G. W. M., Klok H. A.. Advanced drug delivery devices via self-assembly of amphiphilic block copolymers[J]. Adv. Drug Deliv. Rev., 2012, 64(1): 270-279.
-
[20]
Xiong X. B., Binkhathlan Z., Molavi O., Lavasanifar A.. Amphiphilic block co-polymers:Preparation and application in nanodrug and gene delivery[J]. Acta Biomater., 2012, 8(6): 2017-2033. doi: 10.1016/j.actbio.2012.03.006
-
[21]
Aziz Z. A. B. A., Ahmad A., Mohd-Setapar S. H., Hassan H.. Recent advances in drug delivery of polymeric nano-micelles[J]. Curr. Drug Metab., 2017, 18(1): 16-29. doi: 10.2174/1389200217666160921143616
-
[22]
Allain V., Bourgaux C., Couvreur P.. Self-assembled nucleolipids:From supramolecular structure to soft nucleic acid and drug delivery devices[J]. Nucleic Acids Res., 2012, 40(5): 1891-1903. doi: 10.1093/nar/gkr681
-
[23]
Chen Y., Liang G.. Enzymatic self-assembly of nanostructures for theranostics[J]. Theranostics, 2012, 2(2): 139-147. doi: 10.7150/thno.3696
-
[24]
Mai Y., Eisenberg A.. Self-assembly of block copolymers[J]. Chem. Soc. Rev., 2012, 41(18): 5969-5985. doi: 10.1039/c2cs35115c
-
[25]
Kim J. K., Yang S. Y., Lee Y., Kim Y.. Functional nanomaterials based on block copolymer self-assembly[J]. Prog. Polym. Sci., 2010, 35(11): 1325-1349. doi: 10.1016/j.progpolymsci.2010.06.002
-
[26]
Zhang Z., Ma R., Shi L.. Cooperative macromolecular self-assembly toward polymeric assemblies with multiple and bioactive functions[J]. Acc. Chem. Res., 2014, 47(4): 1426-1437. doi: 10.1021/ar5000264
-
[27]
Wu W., Wu D., Li S., Lin Z.. Doxorubicin loaded ph-sensitive micelles for potential tumor therapy[J]. J. Control. Release, 2013, 172(1): E72-E73.
-
[28]
Cheng T., Ma R., Zhang Y., Ding Y.. A surface-adaptive nanocarrier to prolong circulation time and enhance cellular uptake[J]. Chem. Commun., 2015, 51(81): 14985-14988. doi: 10.1039/C5CC05854F
-
[29]
Breus V. V., Heyes C. D., Tron K., Nienhaus G. U.. Zwitterionic biocompatible quantum dots for wide ph stability and weak nonspecific binding to cells[J]. ACS Nano, 2009, 3(9): 2573-2580. doi: 10.1021/nn900600w
-
[30]
Arvizo R. R., Miranda O. R., Thompson M. A., Pabelick C. M.. Effect of nanoparticle surface charge at the plasma membrane and beyond[J]. Nano Lett., 2010, 10(7): 2543-2548. doi: 10.1021/nl101140t
-
[31]
Deshpande M. C., Davies M. C., Garnett M. C., Williams P. M.. The effect of poly(ethylene glycol) molecular architecture on cellular interaction and uptake of DNA complexes[J]. J. Control. Release, 2004, 97(1): 143-156. doi: 10.1016/j.jconrel.2004.02.019
-
[32]
Yuan Y. Y., Mao C. Q., Du X. J., Du J. Z.. Surface charge switchable nanoparticles based on zwitterionic polymer for enhanced drug delivery to tumor[J]. Adv. Mater., 2012, 24(40): 5476-5480. doi: 10.1002/adma.v24.40
-
[33]
Du J. Z., Sun T. M., Song W. J., Wu J.. A tumor-acidity-activated charge-conversional nanogel as an intelligent vehicle for promoted tumoral-cell uptake and drug delivery[J]. Angew. Chem. Int. Ed., 2010, 49(21): 3621-3626. doi: 10.1002/anie.200907210
-
[34]
Xiong M. H., Bao Y., Yang X. Z., Wang Y. C.. Lipase-sensitive polymeric triple-layered nanogel for "on-demand" drug delivery[J]. J. Am. Chem. Soc., 2012, 134(9): 4355-4362. doi: 10.1021/ja211279u
-
[35]
Du J. Z., Du X. J., Mao C. Q., Wang J.. Tailor-made dual ph-sensitive polymer-doxorubicin nanoparticles for efficient anticancer drug delivery[J]. J. Am. Chem. Soc., 2011, 133(44): 17560-17563. doi: 10.1021/ja207150n
-
[36]
Pereverzeva E., Treschalin I., Bodyagin D., Maksimenko O.. Intravenous tolerance of a nanoparticle-based formulation of doxorubicin in healthy rats[J]. Toxicol. Lett., 2008, 178(1): 9-19. doi: 10.1016/j.toxlet.2008.01.020
-
[37]
Harker W. G., Sikic B. I.. Multidrug (pleiotropic) resistance in doxorubicin-selected variants of the human sarcoma cell line mes-sa[J]. Cancer Res., 1985, 45(9): 4091-4096.
-
[38]
Cheng T., Liu J., Ren J., Huang F.. Green tea catechin-based complex micelles combined with doxorubicin to overcome cardiotoxicity and multidrug resistance[J]. Theranostics, 2016, 6(9): 1277-1292. doi: 10.7150/thno.15133
-
[39]
Sharma A., Sharma U. S.. Liposomes in drug delivery:Progress and limitations[J]. Int. J. Pharmaceut., 1997, 154(2): 123-140. doi: 10.1016/S0378-5173(97)00135-X
-
[40]
Wang Y., Miao L., Satterlee A., Huang L.. Delivery of oligonucleotides with lipid nanoparticles[J]. Adv. Drug Deliv. Rev., 2015, 87(1): 68-80.
-
[41]
Goins B., Phillips W. T., Bao A.. Strategies for improving the intratumoral distribution of liposomal drugs in cancer therapy[J]. Expert Opin. Drug Deliv., 2016, 13(6): 873-889.
-
[42]
Sercombe L., Veerati T., Moheimani F., Wu S. Y.. Advances and challenges of liposome assisted drug delivery[J]. Front Pharmacol., 2015, : 6. doi: 10.3389/fphar.2015.00286
-
[43]
Barenholz Y.. Liposome application:Problems and prospects[J]. Curr. Opin. Colloid Interface Sci., 2001, 6(1): 66-77. doi: 10.1016/S1359-0294(00)00090-X
-
[44]
Kraft J. C., Freeling J. P., Wang Z., Ho R. J.. Emerging research and clinical development trends of liposome and lipid nanoparticle drug delivery systems[J]. J. Pharm. Sci., 2014, 103(1): 29-52.
-
[45]
Chang H. I., Yeh M. K.. Clinical development of liposome-based drugs:Formulation, characterization, and therapeutic efficacy[J]. Int. J. Nanomed., 2012, 7(1): 49-60.
-
[46]
Yang F., Jin C., Jiang Y., Li J.. Liposome based delivery systems in pancreatic cancer treatment:From bench to bedside[J]. Cancer Treat Rev., 2011, 37(8): 633-642. doi: 10.1016/j.ctrv.2011.01.006
-
[47]
Mo R., Jiang T., Gu Z.. Recent progress in multidrug delivery to cancer cells by liposomes[J]. Nanomedicine, 2014, 9(8): 1117-1120. doi: 10.2217/nnm.14.62
-
[48]
Immordino M. L., Dosio F., Cattel L.. Stealth liposomes:Review of the basic science, rationale, and clinical applications, existing and potential[J]. Int. J. Nanomed., 2006, 1(3): 297-315. doi: 10.2217/17435889.1.3.297
-
[49]
Wang H., Zhang S., Liao Z., Wang C.. Peglated magnetic polymeric liposome anchored with tat for delivery of drugs across the blood-spinal cord barrier[J]. Biomaterials, 2010, 31(25): 6589-6596. doi: 10.1016/j.biomaterials.2010.04.057
-
[50]
Suntres Z. E.. Liposomal antioxidants for protection against oxidant-induced damage[J]. J. Toxicol., 2011, : . doi: 10.1155/2011/152474
-
[51]
Zhang X., Guo S., Fan R., Yu M.. Dual-functional liposome for tumor targeting and overcoming multidrug resistance in hepatocellular carcinoma cells[J]. Biomaterials, 2012, 33(29): 7103-7114. doi: 10.1016/j.biomaterials.2012.06.048
-
[52]
Wang H., Zhao P., Su W., Wang S.. PLGA/polymeric liposome for targeted drug and gene co-delivery[J]. Biomaterials, 2010, 31(33): 8741-8748. doi: 10.1016/j.biomaterials.2010.07.082
-
[53]
Jiang T., Mo R., Bellotti A., Zhou J.. Gel-liposome-mediated co-delivery of anticancer membrane-associated proteins and small-molecule drugs for enhanced therapeutic efficacy[J]. Adv. Funct. Mater., 2014, 24(16): 2295-2304. doi: 10.1002/adfm.v24.16
-
[54]
Mo R., Jiang T. Y., Gu Z.. Enhanced anticancer efficacy by atp-mediated liposomal drug delivery[J]. Angew. Chem. Int Ed., 2014, 53(23): 5815-5820. doi: 10.1002/anie.201400268
-
[55]
Schafer J., Hobel S., Bakowsky U., Aigner A.. Liposome-polyethylenimine complexes for enhanced DNA and sirna delivery[J]. Biomaterials, 2010, 31(26): 6892-6900. doi: 10.1016/j.biomaterials.2010.05.043
-
[56]
Rengan A. K., Bukhari A. B., Pradhan A., Malhotra R.. In vivo analysis of biodegradable liposome gold nanoparticles as efficient agents for photothermal therapy of cancer[J]. Nano Lett., 2015, 15(2): 842-848. doi: 10.1021/nl5045378
-
[57]
Hubbell J. A., Chilkoti A.. Nanomaterials for drug delivery[J]. Science, 2012, 337(6092): 303-305. doi: 10.1126/science.1219657
-
[58]
Park J. H., Lee S., Kim J. H., Park K.. Polymeric nanomedicine for cancer therapy[J]. Prog. Polym. Sci., 2008, 33(1): 113-137. doi: 10.1016/j.progpolymsci.2007.09.003
-
[59]
Tong R., Cheng J.. Anticancer polymeric nanomedicines[J]. Polym. Rev., 2007, 47(3): 345-381. doi: 10.1080/15583720701455079
-
[60]
Huang P., Wang D., Su Y., Huang W.. Combination of small molecule prodrug and nanodrug delivery:Amphiphilic drug-drug conjugate for cancer therapy[J]. J. Am. Chem. Soc., 2014, 136(33): 11748-56. doi: 10.1021/ja505212y
-
[61]
Hu M., Huang P., Wang Y., Su Y.. Synergistic combination chemotherapy of camptothecin and floxuridine through self-assembly of amphiphilic drug-drug conjugate[J]. Bioconjugate. Chem., 2015, 26(12): 2497-2506. doi: 10.1021/acs.bioconjchem.5b00513
-
[62]
Zhang T., Huang P., Shi L., Su Y.. Self-assembled nanoparticles of amphiphilic twin drug from floxuridine and bendamustine for cancer therapy[J]. Mol. Pharm., 2015, 12(7): 2328-2336. doi: 10.1021/acs.molpharmaceut.5b00005
-
[63]
Ma Y., Mou Q., Sun M., Yu C.. Cancer theranostic nanoparticles self-assembled from amphiphilic small molecules with equilibrium shift-induced renal clearance[J]. Theranostics, 2016, 6(10): 1703-1716. doi: 10.7150/thno.15647
-
[64]
Mou Q., Ma Y., Zhu X., Yan D.. A small molecule nanodrug consisting of amphiphilic targeting ligand-chemotherapy drug conjugate for targeted cancer therapy[J]. J. Control. Release, 2016, 230(1): 34-44.
-
[65]
Wang Y., Huang P., Hu M., Huang W.. Self-delivery nanoparticles of amphiphilic methotrexate-gemcitabine prodrug for synergistic combination chemotherapy via effect of deoxyribonucleotide pools[J]. Bioconjugate. Chem., 2016, 27(11): 2722-2733. doi: 10.1021/acs.bioconjchem.6b00503
-
[66]
Pack D. W., Hoffman A. S., Pun S., Stayton P. S.. Design and development of polymers for gene delivery[J]. Nat. Rev. Drug Discov., 2005, 4(7): 581-93. doi: 10.1038/nrd1775
-
[67]
Xu Z. P., Zeng Q. H., Lu G. Q., Yu A. B.. Inorganic nanoparticles as carriers for efficient cellular delivery[J]. Chem Eng. Sci., 2006, 61(3): 1027-1040. doi: 10.1016/j.ces.2005.06.019
-
[68]
Lacerda L., Raffa S., Prato M., Bianco A.. Cell-penetrating cnts for delivery of therapeutics[J]. Nano Today, 2007, 2(6): 38-43. doi: 10.1016/S1748-0132(07)70172-X
-
[69]
Mao S., Sun W., Kissel T.. Chitosan-based formulations for delivery of DNA and sirna[J]. Adv. Drug Deliv. Rev., 2010, 62(1): 12-27. doi: 10.1016/j.addr.2009.08.004
-
[70]
Chapel J. P., Berret J. F.. Versatile electrostatic assembly of nanoparticles and polyelectrolytes:Coating, clustering and layer-by-layer processes[J]. Curr. Opin. Colloid Interface Sci., 2012, 17(2): 97-105. doi: 10.1016/j.cocis.2011.08.009
-
[71]
Shmueli R. B., Anderson D. G., Green J. J.. Electrostatic surface modifications to improve gene delivery[J]. Expert Opin. Drug Deliv., 2010, 7(4): 535-550. doi: 10.1517/17425241003603653
-
[72]
Mulligan R. C.. The basic science of gene therapy[J]. Science, 1993, 260(5110): 926-32. doi: 10.1126/science.8493530
-
[73]
Liu Y., Du J., Choi J. S., Chen K. J.. A high-throughput platform for formulating and screening multifunctional nanoparticles capable of simultaneous delivery of genes and transcription factors[J]. Angew. Chem. Int. Ed., 2016, 55(1): 169-173. doi: 10.1002/anie.201507546
-
[74]
Verma I. M., Somia N.. Gene therapy-promises, problems and prospects[J]. Nature, 1997, 389(6648): 239-42. doi: 10.1038/38410
-
[75]
Kircheis R., Wightman L., Wagner E.. Design and gene delivery activity of modified polyethylenimines[J]. Adv. Drug Deliv. Rev., 2001, 53(3): 341-358. doi: 10.1016/S0169-409X(01)00202-2
-
[76]
Harris T. J., Green J. J., Fung P. W., Langer R.. Tissue-specific gene delivery via nanoparticle coating[J]. Biomaterials, 2010, 31(5): 998-1006. doi: 10.1016/j.biomaterials.2009.10.012
-
[77]
Liu Y., Wang H., Kamei K. I., Yan M.. Delivery of intact transcription factor by using self-assembled supramolecular nanoparticles[J]. Angew. Chem. Int. Ed., 2011, 50(13): 3058-3062. doi: 10.1002/anie.201005740
-
[78]
Won Y. W., Adhikary P. P., Lim K. S., Kim H. J.. Oligopeptide complex for targeted non-viral gene delivery to adipocytes[J]. Nat. Mater., 2014, 13(12): 1157-1164. doi: 10.1038/nmat4092
-
[79]
Ariga K., Lvov Y. M., Kawakami K., Ji Q.. Layer-by-layer self-assembled shells for drug delivery[J]. Adv. Drug Deliv. Rev., 2011, 63(9): 762-771. doi: 10.1016/j.addr.2011.03.016
-
[80]
Ariga K., Yamauchi Y., Rydzek G., Ji Q.. Layer-by-layer nanoarchitectonics:Invention, innovation, and evolution[J]. Chem Lett., 2014, 43(1): 36-68. doi: 10.1246/cl.130987
-
[81]
Fujii N., Fujimoto K., Michinobu T., Akada M.. The simplest layer-by-layer assembly structure:Best paired polymer electrolytes with one charge per main chain carbon atom for multi layered thin films[J]. Macromolecules, 2010, 43(8): 3947-3955. doi: 10.1021/ma100473j
-
[82]
Lvov Y., Onda M., Ariga K., Kunitake T.. Ultrathin films of charged polysaccharides assembled alternately with linear polyions[J]. J. Biomat. Sci. Polym. E, 1998, 9(4): 345-355. doi: 10.1080/09205063.1998.9753060
-
[83]
Katagiri K., Hamasaki R., Ariga K., Kikuchi J.. Layered paving of vesicular nanoparticles formed with cerasome as a bioinspired organic-inorganic hybrid[J]. J. Am. Chem. Soc., 2002, 124(27): 7892-7893. doi: 10.1021/ja0259281
-
[84]
Elbakry A., Zaky A., Liebkl R., Rachel R.. Layer-by-layer assembled gold nanoparticles for sirna delivery[J]. Nano Lett., 2009, 9(5): 2059-2064. doi: 10.1021/nl9003865
-
[85]
Saurer E. M., Flessner R. M., Sullivan S. P., Prausnitz M. R.. Layer-by-layer assembly of DNA-and protein-containing films on microneedles for drug delivery to the skin[J]. Biomacromolecules, 2010, 11(11): 3136-3143. doi: 10.1021/bm1009443
-
[86]
Morton S. W., Shah N. J., Quadir M. A., Deng Z. J.. Osteotropic therapy via targeted layer-by-layer nanoparticles[J]. Adv. Healthc. Mater., 2014, 3(6): 867-75. doi: 10.1002/adhm.201300465
-
[87]
Shutava T. G., Balkundi S. S., Vangala P., Steffan J. J.. Layer-by-layer-coated gelatin nanoparticles as a vehicle for delivery of natural polyphenols[J]. ACS Nano, 2009, 3(7): 1877-1885. doi: 10.1021/nn900451a
-
[88]
Agarwal A., Lvov Y., Sawant R., Torchilin V.. Stable nanocolloids of poorly soluble drugs with high drug content prepared using the combination of sonication and layer-by-layer technology[J]. J. Control. Release, 2008, 128(3): 255-260. doi: 10.1016/j.jconrel.2008.03.017
-
[89]
Pargaonkar N., Lvov Y. M., Li N., Steenekamp J. H.. Controlled release of dexamethasone from microcapsules produced by polyelectrolyte layer-by-layer nanoassembly[J]. Pharm. Res., 2005, 22(5): 826-835. doi: 10.1007/s11095-005-2600-0
-
[90]
Deng Z. J., Morton S. W., Ben-Akiva E., Dreaden E. C.. Layer-by-layer nanoparticles for systemic codelivery of an anticancer drug and sirna for potential triple-negative breast cancer treatment[J]. ACS Nano, 2013, 7(11): 9571-9584. doi: 10.1021/nn4047925
-
[91]
Poon Z., Chang D., Zhao X., Hammond P. T.. Layer-by-layer nanoparticles with a pH-sheddable layer for in vivo targeting of tumor hypoxia[J]. ACS Nano, 2011, 5(6): 4284-4292. doi: 10.1021/nn200876f
-
[92]
Kim B. S., Park S. W., Hammond P. T.. Hydrogen-bonding layer-by-layer assembled biodegradable polymeric micelles as drug delivery vehicles from surfaces[J]. ACS Nano, 2008, 2(2): 386-392. doi: 10.1021/nn700408z
-
[93]
Ma X., Zhao Y.. Biomedical applications of supramolecular systems based on host-guest interactions[J]. Chem. Rev., 2015, 115(15): 7794-7839. doi: 10.1021/cr500392w
-
[94]
Karim A. A., Dou Q., Li Z., Loh X. J.. Emerging supramolecular therapeutic carriers based on host-guest interactions[J]. Chem. Asian J., 2016, 11(9): 1300-1321. doi: 10.1002/asia.v11.9
-
[95]
Hu J., Liu S.. Engineering responsive polymer building blocks with host-guest molecular recognition for functional applications[J]. Acc. Chem. Res., 2014, 47(7): 2084-2095. doi: 10.1021/ar5001007
-
[96]
Zhang J., Ma P. X.. Cyclodextrin-based supramolecular systems for drug delivery:Recent progress and future perspective[J]. Adv. Drug Deliv. Rev., 2013, 65(9): 1215-1233. doi: 10.1016/j.addr.2013.05.001
-
[97]
Wang L., Li L. L., Fan Y. S., Wang H.. Host-guest supramolecular nanosystems for cancer diagnostics and therapeutics[J]. Adv. Mater., 2013, 25(28): 3888-3898. doi: 10.1002/adma.v25.28
-
[98]
Challa R., Ahuja A., Ali J., Khar R. K.. Cyclodextrins in drug delivery:An updated review[J]. AAPS PharmSciTech., 2005, 6(2): E329-E357. doi: 10.1208/pt060243
-
[99]
Stella V. J., Rajewski R. A.. Cyclodextrins:Their future in drug formulation and delivery[J]. Pharm. Res-Dordr., 1997, 14(5): 556-567. doi: 10.1023/A:1012136608249
-
[100]
Gref R., Amiel C., Molinard K., Daoud-Mahammed S.. New self-assembled nanogels based on host-guest interactions:Characterization and drug loading[J]. J. Control. Release, 2006, 111(3): 316-324. doi: 10.1016/j.jconrel.2005.12.025
-
[101]
Zhang J., Ma P. X.. Polymeric core-shell assemblies mediated by host-guest interactions:versatile nanocarriers for drug delivery[J]. Angew. Chem. Int. Ed., 2009, 48(5): 964-968. doi: 10.1002/anie.v48:5
-
[102]
Hu Q. D., Tang G. P., Chu P. K.. Cyclodextrin-based host-guest supramolecular nanoparticles for delivery:from design to applications[J]. Acc. Chem. Res., 2014, 47(7): 2017-2025. doi: 10.1021/ar500055s
-
[103]
Wang H., Wang S., Su H., Chen K. J.. A supramolecular approach for preparation of size-controlled nanoparticles[J]. Angew. Chem. Int. Ed., 2009, 48(24): 4344-4318. doi: 10.1002/anie.v48:24
-
[104]
Ang C.Y., Tan S. Y., Wang X., Zhang Q.. Supramolecular nanoparticle carriers self-assembled from cyclodextrin-and adamantane-functionalized polyacrylates for tumor-targeted drug delivery[J]. J. Mater. Chem. B, 2014, 2(13): 1879-1890. doi: 10.1039/c3tb21325k
-
[105]
Qu D. H., Wang Q. C., Zhang Q. W., Ma X.. Photoresponsive host-guest functional systems[J]. Chem. Rev., 2015, 115(15): 7543-7588. doi: 10.1021/cr5006342
-
[106]
Dan Z., Cao H., He X., Zeng L.. Biological stimuli-responsive cyclodextrin-based host-guest nanosystems for cancer therapy[J]. Int. J. Pharm., 2015, 483(1-2): 63-68. doi: 10.1016/j.ijpharm.2015.01.035
-
[107]
Zhang W., Li Y., Sun J. H., Tan C. P.. Supramolecular self-assembled nanoparticles for chemo-photodynamic dual therapy against cisplatin resistant cancer cells[J]. Chem. Commun., 2015, 51(10): 1807-1810. doi: 10.1039/C4CC08583C
-
[108]
Wang Y., Li D., Jin Q., Ji J.. pH-responsive supramolecular prodrug micelles based on cucurbit 8 uril for intracellular drug delivery[J]. J Control. Release, 2015, 213(1): E134-E135.
-
[109]
Yu G., Jie K., Huang F.. Supramolecular amphiphiles based on host-guest molecular recognition motifs[J]. Chem. Rev., 2015, 115(15): 7240-7303. doi: 10.1021/cr5005315
-
[110]
Yang B., Dong X., Lei Q., Zhuo R.. Host-guest interaction-based self-engineering of nano-sized vesicles for co-delivery of genes and anticancer drugs[J]. ACS Appl. Mater. Interfaces, 2015, 7(39): 22084-22094. doi: 10.1021/acsami.5b07549
-
[111]
Liu Y., Yu C., Jin H., Jiang B.. A supramolecular janus hyperbranched polymer and its photoresponsive self-assembly of vesicles with narrow size distribution[J]. J. Am. Chem. Soc., 2013, 135(12): 4765-4770. doi: 10.1021/ja3122608
-
[112]
Li Y., Liu Y., Ma R., Xu Y.. A g-quadruplex hydrogel via multicomponent self-assembly:Formation and zero-order controlled release[J]. ACS Appl. Mater. Interfaces, 2017, 9(15): 13056-13067. doi: 10.1021/acsami.7b00957
-
[113]
Zhao L., Qu R., Li A., Ma R.. Cooperative self-assembly of porphyrins with polymers possessing bioactive functions[J]. Chem. Commun., 2016, 52(93): 13543-13555. doi: 10.1039/C6CC05449H
-
[114]
Gu Z., Biswas A., Zhao M., Tang Y.. Tailoring nanocarriers for intracellular protein delivery[J]. Chem. Soc. Rev., 2011, 40(7): 3638-3655. doi: 10.1039/c0cs00227e
-
[115]
Yan M., Ge J., Liu Z., Ouyang P.. Encapsulation of single enzyme in nanogel with enhanced biocatalytic activity and stability[J]. J. Am. Chem. Soc., 2006, 128(34): 11008-11009. doi: 10.1021/ja064126t
-
[116]
Yan M., Du J., Gu Z., Liang M.. A novel intracellular protein delivery platform based on single-protein nanocapsules[J]. Nat. Nanotechnol., 2010, 5(1): 48-53. doi: 10.1038/nnano.2009.341
-
[117]
Gu Z., Yan M., Hu B., Joo K. I.. Protein nanocapsule weaved with enzymatically degradable polymeric network[J]. Nano Lett., 2009, 9(12): 4533-4538. doi: 10.1021/nl902935b
-
[118]
Wen J., Anderson S. M., Du J., Yan M.. Controlled protein delivery based on enzyme-responsive nanocapsules[J]. Adv. Mater., 2011, 23(39): 4549-53. doi: 10.1002/adma.201101771
-
[119]
Liang S., Liu Y., Jin X., Liu G.. Phosphorylcholine polymer nanocapsules prolong the circulation time and reduce the immunogenicity of therapeutic proteins[J]. Nano Res., 2016, 9(4): 1022-1031. doi: 10.1007/s12274-016-0991-3
-
[120]
Zhao M., Hu B., Gu Z., Joo K. I.. Degradable polymeric nanocapsule for efficient intracellular delivery of a high molecular weight tumor-selective protein complex[J]. Nano Today, 2013, 8(1): 11-20. doi: 10.1016/j.nantod.2012.12.003
-
[121]
Tian H., Du J., Wen J., Liu Y.. Growth-factor nanocapsules that enable tunable controlled release for bone regeneration[J]. ACS Nano, 2016, 10(8): 7362-7369. doi: 10.1021/acsnano.5b07950
-
[122]
Liu C., Wen J., Meng Y., Zhang K.. Efficient delivery of therapeutic mirna nanocapsules for tumor suppression[J]. Adv. Mater., 2015, 27(2): 292-297. doi: 10.1002/adma.v27.2
-
[123]
Peer D., Karp J. M., Hong S., FaroKHzad O. C.. Nanocarriers as an emerging platform for cancer therapy[J]. Nat. Nanotechnol., 2007, 2(12): 751-760. doi: 10.1038/nnano.2007.387
-
[124]
Wang M., Thanou M.. Targeting nanoparticles to cancer[J]. Pharmacol. Res., 2010, 62(2): 90-99. doi: 10.1016/j.phrs.2010.03.005
-
[125]
DeSantis C. E., Lin C. C., Mariotto A. B., Siegel R. L.. Cancer treatment and survivorship statistics, ,2014[J]. CA:A Cancer Journal for Clinicians, 2014, 64(4): 252-271. doi: 10.3322/caac.v64.4
-
[126]
Sun T. M., Zhang Y. S., Pang B., Hyun D. C.. Engineered nanoparticles for drug delivery in cancer therapy[J]. Angew. Chem. Int. Ed., 2014, 53(46): 12320-12364.
-
[127]
Liu Y., Li J., Lu Y. F.. Enzyme therapeutics for systemic detoxification[J]. Adv. Drug Deliv. Rev., 2015, 90: 24-39. doi: 10.1016/j.addr.2015.05.005
-
[128]
Bae Y. H., Park K.. Targeted drug delivery to tumors:myths, reality and possibility[J]. J. Control. Release, 2011, 153(3): 198-205. doi: 10.1016/j.jconrel.2011.06.001
-
[129]
LaVan D. A., McGuire T., Langer R.. Small-scale systems for in vivo drug delivery[J]. Nat. Biotechnol., 2003, 21(10): 1184-1191. doi: 10.1038/nbt876
-
[130]
Ganta S., Devalapally H., Shahiwala A., Amiji M.. A review of stimuli-responsive nanocarriers for drug and gene delivery[J]. J. Control. Release, 2008, 126(3): 187-204. doi: 10.1016/j.jconrel.2007.12.017
-
[131]
Wang G., Uludag H.. Recent developments in nanoparticle-based drug delivery and targeting systems with emphasis on protein-based nanoparticles[J]. Expert Opin. Drug Deliv., 2008, 5(5): 499-515. doi: 10.1517/17425247.5.5.499
-
[132]
Gao H., Cheng T., Liu J., Liu J.. Self-regulated multifunctional collaboration of targeted nanocarriers for enhanced tumor therapy[J]. Biomacromolecules, 2014, 15(10): 3634-3642. doi: 10.1021/bm5009348
-
[133]
Shuhendler A. J., Prasad P., Leung M., Rauth A. M.. A novel solid lipid nanoparticle formulation for active targeting to tumor alpha(v)beta(3) integrin receptors reveals cyclic rgd as a double-edged sword[J]. Adv. Healthc. Mater., 2012, 1(5): 600-608. doi: 10.1002/adhm.201200006
-
[134]
Cheng T. J., Ma R. J., Zhang Y. M., Ding Y. X.. A surface-adaptive nanocarrier to prolong circulation time and enhance cellular uptake[J]. Chem. Commun., 2015, 51(81): 14985-14988. doi: 10.1039/C5CC05854F
-
[135]
Falamarzian A., Lavasanifar A.. Optimization of the hydrophobic domain in poly(ethylene oxide)-poly(epsilon-caprolactone) based nano-carriers for the solubilization and delivery of amphotericin b[J]. Colloids and Surfaces B-Biointerfaces, 2010, 81(1): 313-320. doi: 10.1016/j.colsurfb.2010.07.025
-
[136]
Gao H. J., Xiong J., Cheng T. J., Liu J. J.. In vivo biodistribution of mixed shell micelles with tunable hydrophilic/hydrophobic surface[J]. Biomacromolecules, 2013, 14(2): 460-467. doi: 10.1021/bm301694t
-
[137]
Wang H. X., Yang X. Z., Sun C. Y., Mao C. Q.. Matrix metalloproteinase 2-responsive micelle for sirna delivery[J]. Biomaterials, 2014, 35(26): 7622-7634. doi: 10.1016/j.biomaterials.2014.05.050
-
[138]
Sun C. Y., Shen S., Xu C. F., Li H. J.. Tumor acidity-sensitive polymeric vector for active targeted sirna delivery[J]. J. Am. Chem. Soc., 2015, 137(48): 15217-15224. doi: 10.1021/jacs.5b09602
-
[139]
Guan X., Guo Z., Lin L., Chen J.. Ultrasensitive pH triggered charge/size dual-rebound gene delivery system[J]. Nano Lett., 2016, 16(11): 6823-6831. doi: 10.1021/acs.nanolett.6b02536
-
[140]
Wakebayashi D., Nishiyama N., Yamasaki Y., Itaka K.. Lactose-conjugated polyion complex micelles incorporating plasmid DNA as a targetable gene vector system:Their preparation and gene transfecting efficiency against cultured HEPG2 cells[J]. J. Control. Release, 2004, 95(3): 653-664. doi: 10.1016/j.jconrel.2004.01.003
-
[141]
Harada A., Kataoka K.. Pronounced activity of enzymes through the incorporation into the core of polyion complex micelles made from charged block copolymers[J]. J. Control. Release, 2001, 72(1-3): 85-91. doi: 10.1016/S0168-3659(01)00264-4
-
[142]
Dufresne M. H., Leroux J. C.. Study of the micellization behavior of different order amino block copolymers with heparin[J]. Pharm. Res., 2004, 21(1): 160-169. doi: 10.1023/B:PHAM.0000012164.60867.c6
-
[143]
Biswas A., Joo K. I., Liu J., Zhao M. X.. Endoprotease-mediated intracellular protein delivery using nanocapsules[J]. ACS Nano, 2011, 5(2): 1385-1394. doi: 10.1021/nn1031005
-
[144]
Liu Y., Wang H., Kamei K., Yan M.. Delivery of intact transcription factor by using self-assembled supramolecular nanoparticles[J]. Angew. Chem. Int. Ed., 2011, 50(13): 3058-3062. doi: 10.1002/anie.201005740
-
[145]
Govender T., Stolnik S., Xiong C., Zhang S.. Drug-polyionic block copolymer interactions for micelle formation:Physicochemical characterisation[J]. J. Control. Release, 2001, 75(3): 249-258. doi: 10.1016/S0168-3659(01)00353-4
-
[146]
Safra T., Muggia F., Jeffers S., Tsao-Wei D. D.. Pegylated liposomal doxorubicin (doxil):Reduced clinical cardiotoxicity in patients reaching or exceeding cumulative doses of 500 mg/m(2)[J]. Ann Oncol., 2000, 11(8): 1029-1033. doi: 10.1023/A:1008365716693
-
[147]
Cho K. J., Wang X., Nie S. M., Chen Z.. Therapeutic nanoparticles for drug delivery in cancer[J]. Clin. Cancer Res., 2008, 14(5): 1310-1316. doi: 10.1158/1078-0432.CCR-07-1441
-
[148]
Koudelka S., Turanek J.. Liposomal paclitaxel formulations[J]. J. Control. Release, 2012, 163(3): 322-334. doi: 10.1016/j.jconrel.2012.09.006
-
[149]
Lim W. T., Leong S. S., Toh C. K., Ang C. S.. A phase i pharmacokinetic study of a liposomal formulation of paclitaxel administered weekly to Asian patients with solid malignancies[J]. J. Clin. Oncol., 2009, 27(15): 2581.
-
[150]
Markman M.. Pegylated liposomal doxorubicin in the treatment of cancers of the breast and ovary[J]. Expert Opin. Pharmaco., 2006, 7(11): 1469-1474. doi: 10.1517/14656566.7.11.1469
-
[151]
Gaspar M. M., Perez-Soler R., Cruz M. E.. Biological characterization of l-asparaginase liposomal formulations[J]. Cancer Chemother. Pharmacol., 1996, 38(4): 373-377. doi: 10.1007/s002800050497
-
[152]
Felgner P. L., Holm M., Chan H.. Cationic liposome mediated transfection[J]. Proc. West Pharmacol. Soc., 1989, 32: 115-121.
-
[153]
Felgner P. L., Ringold G. M.. Cationic liposome-mediated transfection[J]. Nature, 1989, 337(6205): 387-388. doi: 10.1038/337387a0
-
[154]
Murray K. D., McQuillin A., Stewart L., Etheridge C. J.. Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon[J]. Gene Ther., 1999, 6(2): 190-197. doi: 10.1038/sj.gt.3300743
-
[155]
Kim J. K., Choi S. H., Kim C. O., Park J. S.. Enhancement of polyethylene glycol (PEG)-modified cationic liposomemediated gene deliveries:effects on serum stability and transfection efficiency[J]. J. Pharm. Pharmacol., 2003, 55(4): 453-460. doi: 10.1211/002235702928
-
[156]
Zhu L., Kate P., Torchilin V. P.. Matrix metalloprotease 2-responsive multifunctional liposomal nanocarrier for enhanced tumor targeting[J]. ACS Nano, 2012, 6(4): 3491-3498. doi: 10.1021/nn300524f
-
[157]
Anonymous. Classification and diagnosis of diabetes. Diabetes Care 2015, 38(Suppl. 1), S8-S16.
-
[158]
Craft S.. The role of metabolic disorders in alzheimer disease and vascular dementia:Two roads converged[J]. Arch. Neurol., 2009, 66(3): 300-305.
-
[159]
Canivell S., Gomis R.. Diagnosis and classification of autoimmune diabetes mellitus[J]. Autoimmun. Rev., 2014, 13(4-5): 403-407. doi: 10.1016/j.autrev.2014.01.020
-
[160]
Abdi H., Hosseinpanah F., Azizi F., Hadaegh F.. Screening for dysglycemia:a comment on classification and diagnosis of diabetes in american diabetes association standards of medical care in diabetes-, 2016[J]. Arch. Iran. Med., 2017, 20(6): 389-389.
-
[161]
Yang H., Zhang C., Li C., Liu Y.. Glucose-responsive polymer vesicles templated by alpha-CD/PEG inclusion complex[J]. Biomacromolecules, 2015, 16(4): 1372-1381. doi: 10.1021/acs.biomac.5b00155
-
[162]
Yang H., Ma R., Yue J., Li C.. A facile strategy to fabricate glucose-responsive vesicles via a template of thermo-sensitive micelles[J]. Polym. Chem., 2015, 6(20): 3837-3846. doi: 10.1039/C5PY00170F
-
[163]
Zhao L., Xiao C. S., Wang L. Y., Gai G. Q.. Glucose-sensitive polymer nanoparticles for self-regulated drug delivery[J]. Chem. Commun., 2016, 52(49): 7633-7652. doi: 10.1039/C6CC02202B
-
[164]
Wang B. L., Ma R. J., Liu G., Li Y.. Glucose-responsive micelles from self-assembly of poly(ethylene glycol)-b-poly(acrylic acid-co-acrylamidophenylboronic acid) and the controlled release of insulin[J]. Langmuir, 2009, 25(21): 12522-12528. doi: 10.1021/la901776a
-
[165]
Cambre J. N., Sumerlin B. S.. Biomedical applications of boronic acid polymers[J]. Polymer, 2011, 52(21): 4631-4643. doi: 10.1016/j.polymer.2011.07.057
-
[166]
Liu G., Ma R. J., Ren J., Li Z.. A glucose-responsive complex polymeric micelle enabling repeated on-off release and insulin protection[J]. Soft Matter, 2013, 9(5): 1636-1644. doi: 10.1039/C2SM26690C
-
[167]
Selkoe D. J., Schenk D.. Alzheimer's disease:Molecular understanding predicts amyloid-based therapeutics[J]. Annu. Rev. Pharmacol. Toxicol, 2003, 43: 545-84. doi: 10.1146/annurev.pharmtox.43.100901.140248
-
[168]
Small D. H., Losic D., Martin L. L., Turner B. J.. Alzheimer's disease therapeutics:new approaches to an ageing problem[J]. IUBMB Life., 2004, 56(4): 203-208. doi: 10.1080/15216540410001709211
-
[169]
Anand R., Gill K. D., Mahdi A. A.. Therapeutics of alzheimer's disease:Past, present and future[J]. Neuropharmacology, 2014, 76: 27-50. doi: 10.1016/j.neuropharm.2013.07.004
-
[170]
Rafii M. S.. Preclinical alzheimer's disease therapeutics[J]. J. Alzheimers Dis., 2014, 42(Suppl. 4): S545-S549.
-
[171]
Kelleher-Andersson J.. Discovery of neurogenic, alzheimer's disease therapeutics[J]. Curr. Alzheimer Res., 2006, 3(1): 55-62. doi: 10.2174/156720506775697179
-
[172]
Boada M., Ortiz P., Anaya F., Hernandez I.. Amyloid-targeted therapeutics in alzheimer's disease:Use of human albumin in plasma exchange as a novel approach for a beta mobilization[J]. Drug News Perspect., 2009, 22(6): 325-339. doi: 10.1358/dnp.2009.22.6.1395256
-
[173]
Shvaloff A., Neuman E., Guez D.. Lines of therapeutics research in alzheimer's disease[J]. Psychopharmacol. Bull., 1996, 32(3): 343-352.
-
[174]
Hardy J., Selkoe D. J.. Medicine-he amyloid hypothesis of alzheimer's disease:Progress and problems on the road to therapeutics[J]. Science, 2002, 297(5580): 353-356. doi: 10.1126/science.1072994
-
[175]
Dennis J., Selkoe M. D.. The therapeutics of Alzheimer's disease:Where we stand and where we are heading[J]. Ann. Neurol., 2013, 74(3): 328-336. doi: 10.1002/ana.v74.3
-
[176]
Horwich A. L.. Molecular chaperones in cellular protein folding:The birth of a field[J]. Cell, 2014, 157(2): 285-288. doi: 10.1016/j.cell.2014.03.029
-
[177]
Baneyx F., Thomas J. G.. Collaboration of major and minor molecular chaperones in cellular protein folding[J]. Abstracts of Papers of the American Chemical Society., 2000, 219: U179-U180.
-
[178]
Huang F., Wang J. Z., Qu A. T., Shen L. L.. Maintenance of amyloid beta peptide homeostasis by artificial chaperones based on mixed-shell polymeric micelles[J]. Angew. Chem. Int. Ed., 2014, 53(34): 8985-8990. doi: 10.1002/anie.201400735
-
[179]
Wang J., Song Y., Sun P., An Y.. Reversible interactions of proteins with mixed shell polymeric micelles:Tuning the surface hydrophobic/hydrophilic balance toward efficient artificial chaperones[J]. Langmuir, 2016, 32(11): 2737-2749. doi: 10.1021/acs.langmuir.6b00356
-
[180]
Huang F., Shen L., Wang J., Qu A.. Effect of the surface charge of artificial chaperones on the refolding of thermally denatured lysozymes[J]. ACS Appl. Mater. Interfaces, 2016, 8(6): 3669-3678. doi: 10.1021/acsami.5b08843
-
[181]
Wang J., Yin T., Huang F., Song Y.. Artificial chaperones based on mixed shell polymeric micelles:Insight into the mechanism of the interaction of the chaperone with substrate proteins using forster resonance energy transfer[J]. ACS Appl. Mater. Interfaces, 2015, 7(19): 10238-10249. doi: 10.1021/acsami.5b00684
-
[182]
Watanabe K., Nakamura K., Akikusa S., Okada T.. Inhibitors of fibril formation and cytotoxicity of beta-amyloid peptide composed of KLVFF recognition element and flexible hydrophilic disrupting element[J]. Biochem. Biophys. Res. Commun., 2002, 290(1): 121-124. doi: 10.1006/bbrc.2001.6191
-
[183]
Tjernberg L. O., Naslund J., Lindqvist F., Johansson J.. Arrest of beta-amyloid fibril formation by a pentapeptide ligand[J]. J. Biol. Chem., 1996, 271(15): 8545-8. doi: 10.1074/jbc.271.15.8545
-
[184]
Liu F. F., Du W. J., Sun Y., Zheng J.. Atomistic characterization of binding modes and affinity of peptide inhibitors to amyloid-beta protein[J]. Front. Chem. Sci. Eng., 2014, 8(4): 433-444. doi: 10.1007/s11705-014-1454-6
-
[185]
Qu A. T., Huang F., Li A., Yang H. R.. The synergistic effect between KLVFF and self-assembly chaperones on both disaggregation of beta-amyloid fibrils and reducing consequent toxicity[J]. Chem. Commun., 2017, 53(7): 1289-1292. doi: 10.1039/C6CC07803F
-
[186]
Vonghia L., Leggio L., Ferrulli A., Bertini M.. Acute alcohol intoxication[J]. Eur. J. Intern. Med., 2008, 19(8): 561-567. doi: 10.1016/j.ejim.2007.06.033
-
[187]
Kantrow S. P., Shen Z., Zhang P., Ramsey J.. Acute alcohol intoxication, lung permeability and host defense[J]. Alcohol. Clin. Exp. Res., 2008, 32(6): 172a-172a.
-
[188]
Gerstman M. D., Merry A. F., McIlroy D. R., Hannam J. A.. Acute alcohol intoxication and bispectral index monitoring[J]. Acta Anaesth. Scand., 2015, 59(8): 1015-1021. doi: 10.1111/aas.2015.59.issue-8
-
[189]
Sellers E. M., Kalant H.. Drug-therapy-alcohol intoxication and withdrawal[J]. New Eng. J. of Med., 1976, 294(14): 757-762. doi: 10.1056/NEJM197604012941405
-
[190]
Robertson C. C., Sellers E. M.. Alcohol intoxication and alcohol withdrawal syndrome[J]. Postgrad. Med., 1978, 64(6): 133-138. doi: 10.1080/00325481.1978.11715005
-
[191]
Sellers E. M., Kalant H.. Alcohol intoxication and withdrawal[J]. New. Engl. J. Med., 1976, 294(14): 757-762. doi: 10.1056/NEJM197604012941405
-
[192]
Shpilenya L. S., Muzychenko A. P., Gasbarrini G., Addolorato G.. Metadoxine in acute alcohol intoxication:A double-blind, randomized, placebo-controlled study[J]. Alcohol. Clin. Exp. Res., 2002, 26(3): 340-346. doi: 10.1111/acer.2002.26.issue-3
-
[193]
Liu Y., Du J. J., Yan M., Lau M. Y.. Biomimetic enzyme nanocomplexes and their use as antidotes and preventive measures for alcohol intoxication[J]. Nat. Nanotechnol., 2013, 8(3): 187-192. doi: 10.1038/nnano.2012.264
-
[194]
Munoz-Bonilla A., Fernandez-Garcia M.. Polymeric materials with antimicrobial activity[J]. Prog. Polym. Sci., 2012, 37(2): 281-339. doi: 10.1016/j.progpolymsci.2011.08.005
-
[195]
Pelgrift R. Y., Friedman A. J.. Nanotechnology as a therapeutic tool to combat microbial resistance[J]. Adv. Drug Deliv. Rev., 2013, 65(13-14): 1803-1815. doi: 10.1016/j.addr.2013.07.011
-
[196]
Zhang L., Pornpattananangkul D., Hu C. M. J., Huang C. M.. Development of nanoparticles for antimicrobial drug delivery[J]. Currt. Med. Chem., 2010, 17(6): 585-594. doi: 10.2174/092986710790416290
-
[197]
Zhang Y., Chan H. F., Leong K. W.. Advanced materials and processing for drug delivery:the past and the future[J]. Adv. Drug Deliv. Rev., 2013, 65(1): 104-120. doi: 10.1016/j.addr.2012.10.003
-
[198]
Peltonen L. I., Kinnari T. J., Aarnisalo A. A., Kuusela P.. Comparison of bacterial adherence to polylactides, silicone, and titanium[J]. Acta Oto-Laryngologica, 2007, 127(6): 587-593. doi: 10.1080/00016480600987792
-
[199]
Kornman K. S.. Controlled-release local delivery antimicrobials in periodontics:prospects for the future[J]. J Periodontol., 1993, 64(8 Suppl): 782-791.
-
[200]
Smith A. W.. Biofilms and antibiotic therapy:Is there a role for combating bacterial resistance by the use of novel drug delivery systems?[J]. Adv. Drug Deliv. Rev., 2005, 57(10): 1539-1550. doi: 10.1016/j.addr.2005.04.007
-
[201]
Hittinger M., Juntke J., Kletting S., Schneider-Daum N.. Preclinical safety and efficacy models for pulmonary drug delivery of antimicrobials with focus on in vitro models[J]. Adv. Drug Deliv. Rev., 2015, 85: 44-56. doi: 10.1016/j.addr.2014.10.011
-
[202]
Arthur T. D., Cavera V. L., Chikindas M. L.. On bacteriocin delivery systems and potential applications[J]. Future Microbiol., 2014, 9(2): 235-248. doi: 10.2217/fmb.13.148
-
[203]
Herbrecht R., Denning D. W., Patterson T. F., Bennett J. E.. Voriconazole versus amphotericin b for primary therapy of invasive aspergillosis[J]. New Engl. J. Med., 2002, 347(6): 408-415. doi: 10.1056/NEJMoa020191
-
[204]
Walsh T. J., Teppler H., Donowitz G. R., Maertens J. A.. Caspofungin versus liposomal amphotericin B for empirical antifungal therapy in patients with persistent fever and neutropenia[J]. New Engl. J. Med., 2004, 351(14): 1391-1402. doi: 10.1056/NEJMoa040446
-
[205]
Kim H. J., Jones M. N.. The delivery of benzyl penicillin to staphylococcus aureus biofilms by use of liposomes[J]. J. Liposome Res., 2004, 14(3-4): 123-139. doi: 10.1081/LPR-200029887
-
[206]
Pinto-Alphandary H., Andremont A., Couvreur P.. Targeted delivery of antibiotics using liposomes and nanoparticles:Research and applications[J]. Int. J. Antimicrob. Agents, 2000, 13(3): 155-168. doi: 10.1016/S0924-8579(99)00121-1
-
[207]
Onyeji C. O., Nightingale C. H., Marangos M. N.. Enhanced killing of methicillin-resistant staphylococcus aureus in human macrophages by liposome-entrapped vancomycin and teicoplanin[J]. Infection, 1994, 22(5): 338-342. doi: 10.1007/BF01715542
-
[208]
Schumacher I., Margalit R.. Liposome-encapsulated ampicillin:Physicochemical and antibacterial properties[J]. J. Pharm. Sci., 1997, 86(5): 635-641. doi: 10.1021/js9503690
-
[209]
Huang F., Gao Y., Zhang Y., Cheng T.. Silver-decorated polymeric micelles combined with curcumin for enhanced antibacterial activity[J]. ACS Appl. Mater. Interfaces, 2017, 9(20): 16881-16890.
-
[210]
Chu L., Gao H., Cheng T., Zhang Y.. A charge-adaptive nanosystem for prolonged enhanced in vivo antibiotic delivery[J]. Chem. Commun., 2016, 52(37): 6265-6268. doi: 10.1039/C6CC01269H
-
[211]
Shah L. K., Amiji M. M.. Intracellular delivery of saquinavir in biodegradable polymeric nanoparticles for HIV/AIDS[J]. Pharm. Res., 2006, 23(11): 2638-2645. doi: 10.1007/s11095-006-9101-7
-
[212]
Mosqueira V. C. F., Loiseau P. M., Bories C., Legrand P.. Efficacy and pharmacokinetics of intravenous nanocapsule formulations of halofantrine in plasmodium berghei-infected mice[J]. Antimicrob. Agents Ch., 2004, 48(4): 1222-1228. doi: 10.1128/AAC.48.4.1222-1228.2004
-
[213]
Liu Y., Busscher H. J., Zhao B. R., Li Y.. F[J]. Surface-adaptive, antimicrobially loaded, micellar nanocarriers with enhanced penetration and killing efficiency in staphylococcal biofilms. ACS Nano, 2016, 10(4): 4779-4789.
-
[214]
Li Y. M., Liu G. H., Wang X. R., Hu J. M.. Enzyme-responsive polymeric vesicles for bacterial-strainselective delivery of antimicrobial agents[J]. Angew. Chem. Int. Ed., 2016, 55(5): 1760-1764. doi: 10.1002/anie.201509401
-
[215]
Hasan J., Crawford R. J., Lvanova E. P.. Antibacterial surfaces:the quest for a new generation of biomaterials[J]. Trends Biotechnol., 2013, 31(5): 31-40.
-
[216]
Insua I., Liamas E., Zhang Z. Y., Peacock A. F. A.. Enzyme-responsive polyion complex (PIC) nanoparticles for the targeted delivery of antimicrobial polymers[J]. Polym. Chem., 2016, 7(15): 2684-2690. doi: 10.1039/C6PY00146G
-
[1]
-
扫一扫看文章
计量
- PDF下载量: 0
- 文章访问数: 2118
- HTML全文浏览量: 71

下载: