A novel insulin formulation can keep providing steady levels of insulin for much longer periods in-vivo

Authors: Takenaga M.1; Yamaguchi Y.1; Kitagawa A.1; Ogawa Y.1; Mizushima Y.1; Igarashi R.1

Source: Journal of Pharmacy and Pharmacology, Volume 54, Number 9, 1 September 2002 , pp. 1189-1194(6)

Publisher: Pharmaceutical Press

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Abstract:

We have recently succeeded in preparing insulin-loaded microcapsules that release the insulin in a strictly controlled manner with little initial rapid release in-vitro or in-vivo. We show here the superiority of the best formulation prepared with co-poly(D,L-lactic/glycolic) acids (PLGA) (mean MW 5800, L/G ratio 50:50) with a main diameter of 15 ~ 30 mum in-vivo. When 3.2% insulin-loaded PLGA microcapsules were subcutaneously given as a single dose to streptozotocin-induced hyperglycaemic rats (250 U kg-1), plasma insulin levels gradually increased and constant levels (30.3-94.1 muU mL-1) were sustained. Rats receiving the formulation once a week showed not only steady plasma insulin levels, but also gained weight at a similar speed to normal rats. Meanwhile, daily treatment with Humulin U (25 U kg-1) caused a transient high insulin level (2723.9 muU mL-1 at 1 h) in plasma, but the body weight of the rats was little changed. A pharmacological study in female Cynomolgus monkeys also revealed that the microcapsular formulation provided a flat release of insulin for longer periods and showed no immunogenic activity. In the near future, therefore, this insulin formulation could become very beneficial as a provider of basal insulin levels for insulin-dependent diabetic patients.

Document Type: Research article

Affiliations: 1: Institute of Medical Science, St Marianna University School of Medicine, Kawasaki, Japan

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