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负载L-天冬酰胺酶的聚(丙交酯-共-乙交酯)纳米颗粒的制备:聚合物性质对酶负载量、活性及体外释放的影响

Formulation of L-asparaginase-loaded poly(lactide-co-glycolide) nanoparticles: influence of polymer properties on enzyme loading, activity and in vitro release.

作者信息

Gasper M M, Blanco D, Cruz M E, Alonso M J

机构信息

INETI, IBQTA, Department of Biotechnology, Group of Biochemistry I, Estrada do Paço do Lumiar, Lisboa, Portugal.

出版信息

J Control Release. 1998 Mar 2;52(1-2):53-62. doi: 10.1016/s0168-3659(97)00196-x.

Abstract

This paper describes the preparation and characterisation of poly(lactide-co-glycolide) (PLG) nanoparticles containing the enzyme L-asparaginase. L-Asparaginase was encapsulated in PLG nanospheres using a water-in-oil-in-water solvent evaporation technique. The effect of the copolymer molecular weight and the presence of carboxyl-end groups in the copolymer chain on the physicochemical and in vitro release properties of the nanoparticles was investigated. Results indicated that size, encapsulation efficiency and in vitro release properties (enzymatic activity retention and protein quantification) of the nanoparticles were affected by the PLG molecular weight. As expected, nanoparticles made of high-molecular-weight PLG had a larger size, a higher loading and la slower release rate than those made od a low-molecular-weight PLG. Nevertheless, the most relevant factor affecting the entrapment and release of L-asparaginase from PLG nanoparticles was the presence of free carboxyl-end groups in the PLG chain. The nanoparticles made of PLG with free carboxyl-end groups had a high protein loading (4.86%, w/w) and provided a continuous delivery of the active enzyme for 20 days. However, the enzyme loading was lower (2.65%, w/v) and no active enzyme was detected in the release medium after a 14-day incubation period when nanoparticles were made of PLG with carboxyl-end groups esterified. These results give evidence of the potential of PLG nanospheres for the continuous delivery of L-asparaginase for extended periods of time and show the effect of the PLG chain end-groups in the amount and activity of the enzyme loaded into the nanospheres.

摘要

本文描述了含有L-天冬酰胺酶的聚(丙交酯-共-乙交酯)(PLG)纳米颗粒的制备与表征。采用水包油包水溶剂蒸发技术将L-天冬酰胺酶包封在PLG纳米球中。研究了共聚物分子量和共聚物链中羧基端基的存在对纳米颗粒理化性质和体外释放特性的影响。结果表明,纳米颗粒的尺寸、包封效率和体外释放特性(酶活性保留和蛋白质定量)受PLG分子量的影响。正如预期的那样,由高分子量PLG制成的纳米颗粒比由低分子量PLG制成的纳米颗粒尺寸更大、载药量更高且释放速率更慢。然而,影响L-天冬酰胺酶从PLG纳米颗粒中包封和释放的最相关因素是PLG链中游离羧基端基的存在。由具有游离羧基端基的PLG制成的纳米颗粒具有高蛋白载药量(4.86%,w/w),并能持续释放活性酶20天。然而,当纳米颗粒由羧基端基酯化的PLG制成时,酶载药量较低(2.65%,w/v),在孵育14天后,释放介质中未检测到活性酶。这些结果证明了PLG纳米球在长时间持续递送L-天冬酰胺酶方面的潜力,并显示了PLG链端基对负载到纳米球中的酶的量和活性的影响。

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