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Preparation and Evaluation of Modified Mohs Paste without Starch.
Maho Taguchi1, Masato Shigeyama, Nahomi Ito
1Center for Clinical Pharmacy, Yokohama University of Pharmacy.
Summary
This study improved Mohs paste for palliative cancer treatment by removing starch, enhancing stability and reducing skin damage. The new formulation maintains efficacy while improving physical properties and drug release.
Area of Science:
- Oncology
- Dermatology
- Pharmaceutical Sciences
Background:
- Mohs paste, an external preparation for surgically untreatable malignant tumors, contains zinc hydrochloride and zinc oxide starch.
- Traditional Mohs paste formulation suffers from time-dependent changes in physical properties (hardness, viscoelasticity) and liquefaction due to exudate.
Purpose of the Study:
- To overcome the limitations of conventional Mohs paste by modifying its formulation.
- To investigate a new base for Mohs paste to improve its stability and efficacy in palliative cancer treatment.
Main Methods:
- Modified Mohs paste formulation by excluding starch, identified as the cause of physical instability.
- Utilized macrogol ointment as the base for the modified Mohs paste.
- Evaluated physical properties (hardness, malleability, elongation), water-absorbing capacity, and drug release rate.
Main Results:
- The modified Mohs paste exhibited no significant changes in hardness, malleability, or elongation over time.
- Water-absorbing properties remained equivalent to the original Mohs paste, with sustained hardness after water absorption.
- The modified formulation demonstrated a 1.5-fold increase in drug release rate compared to the original paste.
Conclusions:
- The modified Mohs paste using macrogol ointment offers improved stability and reduced risk of liquefaction-associated skin damage.
- Pre-preparation of the modified Mohs paste is feasible, enhancing its clinical utility.
- The new formulation provides equivalent exudate control and enhanced tissue fixation, suggesting improved palliative care outcomes.