Biodegradable implant and a method for preparation thereof

• US 4,612,009 A
• Filed: 06/11/1985
• Issued: 09/16/1986
• Est. Priority Date: 06/19/1984
• Status: Expired due to Fees

• Current Assignee: Ceskoslovenska akademie ved
• Original Assignee: Ceskoslovenska akademie ved
• Inventors: Drobnik, Jaroslav, Stepankova, Helena
• Primary Examiner(s): YASKO JR, JOHN D
• Application Number:
  US06/743,518
• Time in Patent Office: 462 Days
• Field of Search: 604/891, 604/890, 604/892, 424/14, 424/16, 424/19
• US Class Current: 424/426
• CPC Class Codes: A61K 33/243 Platinum; Compounds thereof
• CPC Class Codes: A61K 9/0024 Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L
• CPC Class Codes: A61K 9/2059 Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin

Abstract

The invention pertains to a biodegradable implant formed from a gel completely decomposable in body, which contains the antitumour medical - diamminedichloroplatinum addition compound (cisplatin) and to a method for preparation of this implant.

An object of the invention is a biodegradable implant, wherein a matrix of the said implant is formed by a starch gel containing 0.2 to 2 wt. % NaCl, plasticized by addition of 1 to 30 wt. % of glycerol, suitably shaped, and contains the homogeneously dispersed microcrystalline cisplatin in the amount of 1 to 15 wt. %.

A method for preparation the implant according to the invention consists in a homogeneous mixing of 1 wt. part of a viscous aqueous solution, obtained by dissolution of 0.4 to 4 wt. % NaCl and conversion of 1 to 6 wt. % of starch to a paste by boiling, with 0.1 to 0.8 wt. parts of glycerol, 0.5 to 1 wt. part of starch, and the required amount of microcrystalline cisplatin, deaeration of the mixture, conversion to a gel in a mould determining the final shape of implant by heating in a boiling-water bath, and, eventually, in hardening by soaking in a water-miscible solvent, advantageously in acetone or ethanol.

An advantage of the implant according to the invention consists in a relatively fast release of cisplatin into surroundings, which is desirable with respect to the mechanism of cisplatin action. Another advantage is the degradability of implant to products natural for body, which have not toxicologic nor immunologic importance.

Claims

1. Biodegradable implant, wherein a matrix of the said implant is formed by a starch gel containing 0.2 to 2 weight percent of sodium chloride, plasticized by addition of 1 to 30 weight percent of glycerol, and suitably shaped, which contains a homogeneously dispersed microcrystalline cisplatin in the amount of 1 to 15 weight percent.

2. Method for preparation of the implant according to claim 1, wherein a viscous aqueous solution, obtained by dissolution 0.4 to 4 weight percent of sodium chloride and conversion of 1 to 6 weight percent of starch to a paste by boiling, is in the amount of one weight part homogeneously mixed with 0.1 to 0.8 weight parts of glycerol, 0.5 to 1 weight part of starch, and the required amount of microcrystalline cisplatin, the mixture is deaerated, transferred into a gel in a mould determining the final shape of implant by heating in a boiling-water bath, and, eventually, hardened by soaking in a solvent miscible with water, advantageously in acetone or ethanol.