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糖尿病大鼠口服和皮下给药后,胆酸钠对载胰岛素聚异丁烯氰基丙烯酸酯纳米球吸收的增强作用。

Enhancement of absorption of insulin-loaded polyisobutylcyanoacrylate nanospheres by sodium cholate after oral and subcutaneous administration in diabetic rats.

作者信息

Radwan M A

机构信息

Department of Clinical Pharmacy, College of Pharmacy, Science and Medical Studies, King Saud University, Riyadh, Saudi Arabia.

出版信息

Drug Dev Ind Pharm. 2001 Oct;27(9):981-9. doi: 10.1081/ddc-100107680.

Abstract

Polyisobutylcyanoacrylate (PIBCA) nanospheres were employed as biodegradable polymeric carriers for oral (p.o.) and subcutaneous (s.c.) delivery of insulin. The polymerization technique used was able to hold 65%-95% of insulin added 30 min after initiation of polymerization. The percentage drug loading was monomer concentration dependent. Insulin adsorption to the nanospheres was measured by radioimmunoassay. Although Pluronic F68 (0.5%) did not significantly alter the in vitro insulin degradation half-life T50%, sodium cholate (0.5%) increased the degradation T50% of insulin by 56% (from 13.6 +/- 1.6 to 22.1 +/- 2 min). This study also investigated the in vivo performance of insulin-loaded PIBCA in aqueous suspension with or without sodium cholate (0.5%) and Pluronic F68 (0.5%) surfactants after oral and subcutaneous administration to alloxan-induced diabetic rats. Insulin absorption was evaluated by its hypoglycemic effect. Insulin associated with PIBCA nanospheres retains its biological activity up to 15 h and 24 h after oral and subcutaneous administrations, respectively. Administered orally insulin-loaded (75 U/kg) nanospheres, in the presence of surfactants, significantly reduced the mean blood glucose level from 392 +/- 32 to 80 +/- 13 mg/dl within 2 h and maintained it at 100 mg/dl or less for more than 8 h. On the other hand, the subcutaneous administration of insulin-loaded (25 U/kg) nanospheres significantly decreased the blood glucose level from 406 +/- 33 to 88.5 +/- 12.8 mg/dl within 1 h, and the lowered glucose level was maintained at 100 mg/dl or less for more than 12 h; it returned to its initial value 24 h after administration. Insulin-loaded nanospheres with surfactants showed significant (P < .05) pharmacological availability (PA%) of 37.6% +/- 3.7% and 65.2% +/- 2.7% after oral and subcutaneous dosages, respectively. The existence of surfactants with PIBCA nanospheres improved the oral PA% by 49.2%. These findings suggest that the developed PIBCA, in the presence of surfactants, would be useful not only in improving insulin gastrointestinal absorption, but also in sustaining its systemic action by lowering the blood glucose to an acceptable level.

摘要

聚异丁基氰基丙烯酸酯(PIBCA)纳米球被用作胰岛素口服(p.o.)和皮下(s.c.)给药的可生物降解聚合物载体。所采用的聚合技术能够在聚合开始30分钟后保留65%-95%添加的胰岛素。载药量百分比取决于单体浓度。通过放射免疫测定法测量胰岛素对纳米球的吸附。虽然普朗尼克F68(0.5%)没有显著改变体外胰岛素降解半衰期T50%,但胆酸钠(0.5%)使胰岛素的降解T50%增加了56%(从13.6±1.6分钟增加到22.1±2分钟)。本研究还调查了在给四氧嘧啶诱导糖尿病大鼠口服和皮下给药后,含或不含胆酸钠(0.5%)和普朗尼克F68(0.5%)表面活性剂的载胰岛素PIBCA水悬浮液的体内性能。通过其降血糖作用评估胰岛素吸收情况。与PIBCA纳米球结合的胰岛素在口服和皮下给药后分别在15小时和24小时内保持其生物活性。口服载胰岛素(75 U/kg)纳米球,在表面活性剂存在下,2小时内平均血糖水平从392±32显著降低至80±13 mg/dl,并在8小时以上维持在100 mg/dl或更低。另一方面,皮下注射载胰岛素(25 U/kg)纳米球1小时内血糖水平从406±33显著降低至88.5±12.8 mg/dl,降低的血糖水平在12小时以上维持在100 mg/dl或更低;给药24小时后恢复到初始值。含表面活性剂的载胰岛素纳米球口服和皮下给药后分别显示出显著(P<0.05)的药理利用率(PA%),分别为37.6%±3.7%和65.2%±2.7%。表面活性剂与PIBCA纳米球的存在使口服PA%提高了49.2%。这些发现表明,所开发的PIBCA在表面活性剂存在下不仅有助于改善胰岛素的胃肠道吸收,还能通过将血糖降低到可接受水平来维持其全身作用。

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