[1] 梅兴国.生物技术药物制剂基础与应用[M].北京:化学工业出版社,2004.
[2] 张鲁明,赵秀杰.多肽蛋白药物制药研究的几个热点[J].中国药师,2004,7(9):674.
[3] Rao SV,Yajurvedi K,Shao J.Self-nanoemulsifying drug delivery system (SNEDDS) for oral delivery of protein drugs: III. In vivo oral absorption study.Int J Pharm. 2008;362(1-2): 16-19.
[4] Lyons KC,Charman WN,Miller R,et al.Factors limiting the oral bioavailability of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) and enhancement of absorption in rats by delivery in a water-in-oil microemulsion.Int J Pharm.2000; 199(1):17-28.
[5] Tobío M,Sánchez A,Vila A,et al.The role of PEG on the stability in digestive fluids and in vivo fate of PEG-PLA nanoparticles following oral administration.Colloids Surf B Biointerfaces. 2000;18(3-4):315-323.
[6] 王宝江,杨爽,李丹.蛋白口服给药的研究进展[J].中国医药导刊, 2008,10(8):1236-1237.
[7] 黄建,高春生,梅兴国.多肽和蛋白类药物口服给药给药的可行性探讨[J].国际药学研究杂志,2007,34(3):298-300.
[8] Desai MP,Labhasetwar V,Amidon GL,et al.Gastrointestinal Uptake of Biodegradable Microparticles: Effect of Particle Size.Pharm Res.1996;13(12):1838-1845.
[9] 纳米技术在新药研发中的应用.生命经纬.[2006-4-5]. http:// biox.cn/ content/ 2006405/42830.
[10] des Rieux A,Fievez V,Garinot M,et al.Nanoparticles as potential oral delivery systems of proteins and vaccines: a mechanistic approach. J Control Release. 2006;116(1):1-27.
[11] Yoncheva K, Lizarraga E, Irache JM.Pegylated nanoparticles based on poly(methyl vinyl ether-co-maleic anhydride): preparation and evaluation of their bioadhesive properties.Eur J Pharm Sci.2005;24(5):411-419.
[12] Takeuchi H, Thongborisute J, Matsui Y,et al.Novel mucoadhesion tests for polymers and polymer-coated particles to design optimal mucoadhesive drug delivery systems. Adv Drug Deliv Rev.2005;57(11):1583-1594.
[13] 蒋刚彪,方羽生,高永峰.聚合物胶束作为药物载体的应用[J].现代化工,2007,27(10):69-71.
[14] Goldstein IJ,Hughes RC,Monsigny M,et al.What should be called a lectin?Nature.1987;285:66.
[15] Irache JM, Durrer C, Duchêne D,et al.Preparation and characterization of lectin-latex conjugates for specific bioadhesion.Biomaterials.1994;15(11):899-904.
[16] Irache JM, Durrer C, Duchêne D,et al.Bioadhesion of lectin-latex conjugates to rat intestinal mucosa.Pharm Res. 1996;13(11):1716-1719.
[17] Garinot M,Fiévez V,Pourcelle V,et al.PEGylated PLGA-based nanoparticles targeting M cells for oral vaccination.J Control Release.2007;120(3):195-204.
[18] Kim WJ,Yockman JW,Lee M,et al.Soluble Flt-1 gene delivery using PEI-g-PEG-RGD conjugate for anti-angiogenesis.J Control Release.2005;106(1-2):224-234.
[19] Bharali DJ,Sahoo SK,Mozumdar S,et al.Cross-linked polyvinylpyrrolidone nanoparticles: a potential carrier for hydrophilic drugs.J Colloid Interface Sci.2003;258(2): 415-423.
[20] Chipper NG,Vaum KM,Artursson P.Chitosans as absorption enhancers for poorly absorbable drugs. 1: Infuence of molecular weight and degree of acetylation on drug transport across human intestinal epithelial (Caco-2) cells.Pharm Res.1996;13: 1686-1692.
[21] Calvo P,Remuñan-López C,Vila-Jato JL,et al.Chitosan and chitosan/ethylene oxide-propylene oxide block copolymer nanoparticles as novel carriers for proteins and vaccines. Pharm Res.1997;14(10):1431-1436.
[22] Calvo P,Remunan-Lopez C,Vila-Jato JL,et al.Novel hydrophilic chitosan –polyethylene oxide nanoparticles as protein carriers.Appl Polym Sci.1997;63: 125-132.
[23] Amidi M,Romeijn SG,Borchard G,et al.Preparation and characterization of protein-loaded N-trimethyl chitosan nanoparticles as nasal delivery system.J Control Release. 2006;111(1-2):107-116.
[24] Jaganathan KS,Rao YU,Singh P,et al.Development of a single dose tetanus toxoid formulation based on polymeric microspheres: a comparative study of poly(D,L-lactic-co- glycolic acid) versus chitosan microspheres.Int J Pharm. 2005;294(1-2):23-32.
[25] Bhang SH,Lee TJ,Lim JM,et al.The effect of the controlled release of nerve growth factor from collagen gel on the efficiency of neural cell culture.Biomaterials. 2009; 30(1):126-132.
[26] 章怡彬,梁文权,高建青.纳米粒作为抗肿瘤药物载体的研究进展[J].医学导报,2006,25(6):551-553.
[27] Merdan T,Kopeek J,Kissel T.Prospects for cationic polymers in gene and oligonucleotide therapy against cancer.Adv Drug Del Rev.2002;54:715-758.
[28] Liang HF,Chen CT,Chen SC,et al.Paclitaxel-loaded poly ( g- glutamic acid )- poly (lactide) nanoparticle release a targeted drug delivery system for the treatment of liver cancer. Biomaterials.2006;27:2051-2069.
[29] Li W,Feng SS,Guo YL.Block copolymer micelles for nanomedicine.Nanomedicine.2012;7(2):169-172.
[30] Li W,Nakayama M,Akimoto J,et al.Effect of block compositions of amphiphilic block copolymers on the physicochemical properties of polymeric micelles. Polymer. 2011;52:3783-3790.
[31] Zhang Y, Wu X, Meng L,et al.Thiolated Eudragit nanoparticles for oral insulin delivery: preparation, characterization and in vivo evaluation.Int J Pharm. 2012;436(1-2):341-350.
[32] Wang J,Gao PP.Real-time imaging of intracellular drug release from mesoporous silica nanoparticles based on fluorescence resonance energy transfer.J Mater Chem B. 2014; 2: 4379-4386.
[33] 谢向阳,林雯,李旸,等.刺激响应型纳米药物递送系统设计与构建研究进展[J].国际药学研究杂志,2013,40(5):584-587.
[34] Wang XQ,Zhang Q.pH-sensitive polymeric nanoparticles to improve oral bioavailability of peptide/protein drugs and poorly water-soluble drugs.Eur J Pharm Biopharm. 2012; 82(2):219-229.
[35] Wu H,Zhu L,Torchilin VP.pH-sensitive poly(histidine)-PEG/ DSPE-PEG co-polymer micelles for cytosolic drug delivery. Biomaterials.2013;34(4):1213-1222.
[36] 王志昆,张欢,孙晓岩,等.自组装白蛋白纳米粒的制备及体外释药行为[J].中国药剂学杂志,2014,12(4):115-121.
[37] 张波,张娜.纳米载体共递送化疗药物用于肿瘤联合治疗的研究进展[J].中国新药杂志,2014,23(21):2514-2519. |