Insulin-albumin microbeads: an implantable, biodegradable system.

M F Goosen, Y F Leung, S Chou, A M Sun
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引用次数: 31

Abstract

A feasibility study on developing an implantable, biodegradable insulin delivery system was carried out. Insulin-albumin microbeads (50-1,000 microns diameter) were implanted in diabetic rats. After a single subcutaneous implant of the glutaraldehyde crosslinked microbeads, elevated blood-insulin levels were detected in the diabetic animals for longer than two months. While the blood-insulin levels of the treated animals were sustained between 10 and 67 microU/ml during the initial two month post-implantation period, complete in-vivo biodegradation of the microbeads took longer than five months. The diabetic animals, with the insulin-albumin microbead implants, gained weight. In contrast, untreated diabetic controls lost weight. Fibrous capsules were found to have surrounded the microbeads when the implants were recovered at one and two months post-implantation. The results suggest that the fibrous capsules played a role in retarding insulin release from the albumin microbead system. Cross-linked serum albumin microbeads have the clinical potential of providing long-term in-vivo drug release. This system has the additional advantage of being biodegradable and also provides more options for the method and site of implantation.

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胰岛素-白蛋白微珠:一种可植入的可生物降解系统。
研究了一种可植入、可生物降解的胰岛素输送系统的可行性。将胰岛素白蛋白微球(直径50 ~ 1000微米)植入糖尿病大鼠体内。在单次皮下植入戊二醛交联微珠后,糖尿病动物的血液胰岛素水平升高超过两个月。虽然在植入后的最初两个月,治疗动物的血液胰岛素水平维持在10至67微u /ml之间,但微珠在体内的完全生物降解需要超过5个月的时间。植入胰岛素-白蛋白微珠的糖尿病动物体重增加。相比之下,未经治疗的糖尿病控制组体重下降。当植入后1个月和2个月恢复植入物时,发现纤维囊包围了微珠。结果表明,纤维囊具有延缓胰岛素从白蛋白微珠系统释放的作用。交联血清白蛋白微珠具有提供长期体内药物释放的临床潜力。该系统具有可生物降解的额外优点,也为植入方法和位置提供了更多选择。
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