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Evaluation of lincomycin as a cholesterol gallstone dissolution rate accelerator
Journal of Pharmaceutical Sciences
|June 1, 1985
Summary
Lincomycin hydrochloride accelerated cholesterol gallstone dissolution in vitro, but not in vivo. This suggests interfacial resistance is not the sole factor limiting gallstone dissolution, with mixing also playing a critical role.
Area of Science:
- Gastroenterology
- Pharmacology
- Biochemistry
Background:
- Cholesterol gallstone dissolution is a complex process.
- Interfacial resistance between gallstones and bile may limit dissolution rates.
Purpose of the Study:
- To investigate the role of interfacial resistance in cholesterol gallstone dissolution.
- To determine if lincomycin hydrochloride can enhance gallstone dissolution by reducing interfacial resistance.
Main Methods:
- In vitro dissolution of cholesterol monohydrate pellets in dog bile with and without lincomycin hydrochloride.
- In vivo infusion of lincomycin hydrochloride into dog gallbladders followed by cholesterol pellet dissolution assessment.
Main Results:
- Lincomycin hydrochloride accelerated cholesterol pellet dissolution in vitro.
- No significant alteration in dissolution rate was observed in vivo despite comparable drug concentrations.
Conclusions:
- Interfacial resistance can be reduced by lincomycin hydrochloride in vitro, enhancing dissolution.
- Interfacial resistance is not the sole rate-limiting factor for in vivo gallstone dissolution; other factors like bile mixing are critical.