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由生物相容性微乳液制备可生物降解的胰岛素纳米胶囊。

Preparation of biodegradable insulin nanocapsules from biocompatible microemulsions.

作者信息

Watnasirichaikul S, Davies N M, Rades T, Tucker I G

机构信息

Formulation and Drug Delivery Group, School of Pharmacy, University of Otago, Dunedin, New Zealand.

出版信息

Pharm Res. 2000 Jun;17(6):684-9. doi: 10.1023/a:1007574030674.

Abstract

PURPOSE

To prepare poly(ethyl 2-cyanoacrylate) nanocapsules containing insulin by interfacial polymerization of spontaneously forming, biocompatible microemulsions.

METHODS

A pseudo-ternary phase diagram of a mixture of medium chain glycerides (caprylic/capric triglycerides and mono-/diglycerides), a mixture of surfactants (polysorbate 80 and sorbitan mono-oleate) and water was constructed. Polarizing light microscopy was used to identify combinations forming microemulsions. Microemulsions were characterized by conductivity and viscosity to select systems suitable for the preparation of poly(ethyl 2-cyanoacrylate) nanocapsules by interfacial polymerization. Nanocapsules were prepared by addition of 100 mg of ethyl 2-cyanoacrylate to a stirred water-in-oil microemulsion containing 1 g of water, 7.6 g of oil, and 1.4 g of surfactant. The nanocapsules formed were characterized by photon correlation spectroscopy, freeze fracture transmission and scanning electron microscopy. Insulin nanocapsules were prepared by using an aqueous solution of insulin (100 units/ml) as the dispersed phase of the microemulsion. The entrapment and the release of insulin from the nanocapsules were determined.

RESULTS

Three regions were identified in the pseudo-ternary phase diagram; a microemulsion region, a region in which liquid crystalline structures were present and a coarse emulsion region. All systems in the microemulsion region were water-in-oil dispersions. Poly(ethyl 2-cyanoacrylate) nanocapsules having a mean particle size of 150.9 nm were formed upon interfacial polymerization of the microemulsion. Nanocapsules were found to have a central cavity surrounded by a polymer wall. In excess of 80% of the insulin present in the microemulsion was encapsulated upon interfacial polymerization.

CONCLUSIONS

Interfacial polymerization of spontaneously forming water-in-oil microemulsions represents a convenient method for the preparation of poly(alkylcyanoacrylate) nanocapsules suitable for the entrapment of bioactive peptides.

摘要

目的

通过自发形成的生物相容性微乳液的界面聚合制备含胰岛素的聚(2-氰基丙烯酸乙酯)纳米囊。

方法

构建中链甘油酯(辛酸/癸酸甘油三酯和单/双甘油酯)混合物、表面活性剂混合物(聚山梨酯80和脱水山梨醇单油酸酯)与水的伪三元相图。用偏光显微镜鉴定形成微乳液的组合。通过电导率和粘度对微乳液进行表征,以选择适合通过界面聚合制备聚(2-氰基丙烯酸乙酯)纳米囊的体系。通过向含有1 g水、7.6 g油和1.4 g表面活性剂的搅拌油包水微乳液中加入100 mg 2-氰基丙烯酸乙酯来制备纳米囊。通过光子相关光谱、冷冻断裂透射和扫描电子显微镜对形成的纳米囊进行表征。通过使用胰岛素水溶液(100单位/ml)作为微乳液的分散相来制备胰岛素纳米囊。测定胰岛素从纳米囊中的包封率和释放率。

结果

在伪三元相图中确定了三个区域;一个微乳液区域、一个存在液晶结构的区域和一个粗乳液区域。微乳液区域中的所有体系均为油包水型分散体。微乳液的界面聚合形成了平均粒径为150.9 nm的聚(2-氰基丙烯酸乙酯)纳米囊。发现纳米囊具有被聚合物壁包围的中心腔。微乳液中超过80%的胰岛素在界面聚合时被包封。

结论

自发形成的油包水微乳液的界面聚合是制备适合包封生物活性肽的聚(烷基氰基丙烯酸酯)纳米囊的便捷方法。

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