Tjandrawinata Raymond R, Trisina Jessica, Rahayu Puji, Prasetya Lorentius Agung, Hanafiah Aang, Rachmawati Heni
Dexa Laboratories of Biomolecular Sciences, Dexa Medica, Cikarang, Indonesia.
National Nuclear Energy Agency, Bandung, Indonesia.
Drug Des Devel Ther. 2014 Sep 25;8:1585-93. doi: 10.2147/DDDT.S66007. eCollection 2014.
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, (99m)Tc-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.
DLBS1033是从赤子爱胜蚓中分离出的一种生物活性蛋白组分,当暴露于胃肠道环境时往往不稳定。因此,需要进行适当的药物研发,以最大限度地提高该蛋白组分在胃肠道中的吸收。进行了体外、离体和体内稳定性试验,以研究该生物活性蛋白组分在胃部条件下的稳定性。发现生物活性蛋白组分DLBS1033在低pH值和胃液中不稳定。“肠溶包衣”制剂在类似胃液的介质中无渗漏,在模拟肠液介质中具有良好的释放曲线。经十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)分析证实,DLBS1033以完整蛋白形式通过小肠吸收。该结果证实,使用甲基丙烯酸共聚物的肠溶包衣配方可通过防止DLBS1033在胃中释放,使其免受胃部酸性条件的影响,同时在到达肠道时促进其释放。从血药浓度-时间曲线来看,(99m)Tc-DLBS1033的循环半衰期为70分钟。这种相对较长的生物半衰期支持了其作为溶栓蛋白的功能。因此,肠溶给药系统被认为是DLBS1033作为口服溶栓剂的最佳途径。