Abstract
The initial stages of the in vitro degradation of and the drug release from a matrix made of poly(d,l-lactide-co-glycolide) was carried out in a phosphate buffer saline (pH 7.0) medium. It has been observed that substantial matrix degradation occurs at the end of 2 weeks of immersion. The drug release using films of the polymer shows a tri-phasic pattern, unlike the bi-phasic patterns usually seen. Mechanisms are proposed for each phase of release, based on results from weight loss, amount of water absorption and scanning electron microscopy. The details of the structural changes and their effects on drug release may have implications for delivering potent drugs over a 2-week period.
MeSH terms
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Absorbable Implants*
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Absorption
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Biocompatible Materials / chemical synthesis
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Biocompatible Materials / chemistry
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Diffusion
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Drug Carriers / chemical synthesis
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Drug Carriers / chemistry*
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Drug Implants / chemical synthesis
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Drug Implants / chemistry*
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Kinetics
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Lactic Acid / chemistry*
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Materials Testing*
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Membranes, Artificial*
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Metoclopramide / administration & dosage
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Metoclopramide / chemistry*
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Phosphates / chemistry
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Polyglycolic Acid / chemistry*
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Polylactic Acid-Polyglycolic Acid Copolymer
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Polymers / chemistry*
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Transition Temperature
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Water / chemistry*
Substances
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Biocompatible Materials
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Drug Carriers
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Drug Implants
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Membranes, Artificial
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Phosphates
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Polymers
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Water
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Polylactic Acid-Polyglycolic Acid Copolymer
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Polyglycolic Acid
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Lactic Acid
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Metoclopramide