首页> 外文期刊>Drug Design, Development and Therapy >Bioactive protein fraction DLBS1033 containing lumbrokinase isolated from Lumbricus rubellus: ex vivo, in vivo, and pharmaceutic studies
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Bioactive protein fraction DLBS1033 containing lumbrokinase isolated from Lumbricus rubellus: ex vivo, in vivo, and pharmaceutic studies

机译:从rub虫中分离出的含有激酶的生物活性蛋白级分DLBS1033:离体,体内和药物研究

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Abstract: DLBS1033 is a bioactive protein fraction isolated from Lumbricus rubellus that tends to be unstable when exposed to the gastrointestinal environment. Accordingly, appropriate pharmaceutical development is needed to maximize absorption of the protein fraction in the gastrointestinal tract. In vitro, ex vivo, and in vivo stability assays were performed to study the stability of the bioactive protein fraction in gastric conditions. The bioactive protein fraction DLBS1033 was found to be unstable at low pH and in gastric fluid. The “enteric coating” formulation showed no leakage in gastric fluid–like medium and possessed a good release profile in simulated intestinal medium. DLBS1033 was absorbed through the small intestine in an intact protein form, confirmed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE) analysis. This result confirmed that an enteric coating formula using methacrylic acid copolymer could protect DLBS1033 from the acidic condition of the stomach by preventing the release of DLBS1033 in the stomach, while promoting its release when reaching the intestine. From the blood concentration–versus-time curve, 99mTc-DLBS1033 showed a circulation half-life of 70 minutes. This relatively long biological half-life supports its function as a thrombolytic protein. Thus, an enteric delivery system is considered the best approach for DLBS1033 as an oral thrombolytic agent.
机译:摘要:DLBS1033是一种从rub虫中分离出来的生物活性蛋白组分,当暴露于胃肠道环境时往往不稳定。因此,需要适当的药物开发以最大化胃肠道中蛋白质部分的吸收。进行体外,离体和体内稳定性测定法以研究生物活性蛋白级分在胃条件下的稳定性。发现生物活性蛋白级分DLBS1033在低pH和胃液中不稳定。 “肠溶衣”配方在类似胃液的介质中没有泄漏,并且在模拟肠介质中具有良好的释放特性。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS PAGE)分析证实,DLBS1033以完整的蛋白质形式通过小肠吸收。该结果证实,使用甲基丙烯酸共聚物的肠溶衣配方可以通过防止DLBS1033在胃中的释放而在到达肠道时促进其释放,从而保护DLBS1033免受胃的酸性条件的伤害。从血药浓度-时间曲线,99mTc-DLBS1033的循环半衰期为70分钟。这种相对较长的生物学半衰期支持其作为溶栓蛋白的功能。因此,肠内给药系统被认为是DLBS1033作为口服溶栓剂的最佳方法。

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