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羧甲基黄原胶微粒对牛血清白蛋白的可控递送

Controlled delivery of bovine serum albumin from carboxymethyl xanthan microparticles.

作者信息

Maiti Sabyasachi, Ray Somasree, Sa Biswanath

机构信息

Department of Pharmaceutical Technology, Centre for Advanced Research in Pharmaceutical Sciences, Jadavpur University, Kolkata, India.

出版信息

Pharm Dev Technol. 2009;14(2):165-72. doi: 10.1080/10837450802498878.

Abstract

Bovine serum albumin (BSA)-loaded carboxymethyl xanthan (CMX) microparticles were prepared following gelation of sodium carboxymethyl xanthan (SCMX) gum with different concentrations (1-5%) of aluminium chloride (AlCl3). The microparticles prepared using 1% AlCl3 were subsequently coated with 0.5% aqueous solution of either SCMX gum or sodium alginate. Both uncoated and coated microparticles were characterized for entrapment efficiency, surface morphology, particle size, in vitro release and protein stability. The uncoated microparticles became non-spherical and the mean diameter was found to increase with increasing AlCl3 concentration. Higher concentration of AlCl3 decreased BSA entrapment efficiency of the uncoated microparticles from 86-61%. Furthermore, BSA entrapment in coated microparticles was found lower (78-79%) than uncoated microparticles prepared using 1% AlCl3. Although, the uncoated microparticles released almost half of its content in NaCl-HCl buffer solution (pH 1.2) in 2 h, the alginate and xanthan coated microparticles did not liberate a substantial amount of entrapped protein within the same period and prolonged the release in PBS solution (pH 7.4) up to 10 and 12 h, respectively. The microparticles released the protein via diffusion and swelling of the polymer matrix. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that BSA integrity was well retained in the CMX microparticles.

摘要

通过用不同浓度(1 - 5%)的氯化铝(AlCl₃)使羧甲基黄原胶(SCMX)凝胶化,制备了负载牛血清白蛋白(BSA)的羧甲基黄原胶(CMX)微粒。随后,使用1% AlCl₃制备的微粒用0.5%的SCMX胶或海藻酸钠水溶液进行包衣。对未包衣和包衣的微粒进行了包封率、表面形态、粒径、体外释放和蛋白质稳定性的表征。未包衣的微粒变得非球形,并且发现平均直径随着AlCl₃浓度的增加而增大。较高浓度的AlCl₃使未包衣微粒的BSA包封率从86%降至61%。此外,发现包衣微粒中的BSA包封率(78 - 79%)低于使用1% AlCl₃制备的未包衣微粒。尽管未包衣的微粒在2小时内在NaCl - HCl缓冲溶液(pH 1.2)中释放了几乎一半的内容物,但海藻酸钠和黄原胶包衣的微粒在同一时期内没有释放大量包封的蛋白质,并且在PBS溶液(pH 7.4)中的释放时间分别延长至10小时和12小时。微粒通过聚合物基质的扩散和溶胀释放蛋白质。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳表明,BSA的完整性在CMX微粒中得到了很好的保留。

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