Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Chem Pharm Bull (Tokyo) ; 69(2): 211-217, 2021 Feb 01.
Article in English | MEDLINE | ID: mdl-33298636

ABSTRACT

As a result of the research activities of the Japan Agency for Medical Research and Development (AMED), this document aims to show an approach to establishing control strategy for continuous manufacturing of oral solid dosage forms. The methods of drug development, technology transfer, process control, and quality control used in the current commercial batch manufacturing would be effective also in continuous manufacturing, while there are differences in the process development using continuous manufacturing and batch manufacturing. This document introduces an example of the way of thinking for establishing a control strategy for continuous manufacturing processes.


Subject(s)
Dosage Forms , Drug Compounding/methods , Administration, Oral , Dosage Forms/standards , Drug Compounding/standards , Manufacturing Industry/standards , Quality Control
2.
J Pharm Pharmacol ; 55(4): 435-41, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12803764

ABSTRACT

Curdlan jelly was prepared by heating an aqueous curdlan suspension at 70 degrees C for 5 min. Theophylline, as a model drug, was entrapped in the jelly network. Curdlan jelly had a hardness comparable with that of commercially available jelly for confectionary. Syneresis was observed for 8 days after the preparation and was not detected during the experimental term from the gel prepared from 10% w/v curdlan suspension. Release of theophylline from the jellies was sustained, and was increasingly delayed with an increase in the curdlan concentration. An aqueous curdlan suspension was studied by means of differential scanning calorimetry (DSC) up to 80 degrees C and down to -25 degrees C, and subsequent re-heating to 30 degrees C. Enthalpy increased with the concentration of curdlan, while the temperature at the onset of the endothermic peak decreased with the concentration of curdlan. The enthalpy due to thermal gelation of 1 mg curdlan was 12.2 mJ. An increase in curdlan concentration decreased the enthalpy and lowered the onset temperature of the endothermic peak during the DSC re-heating scan. The results are due to an increase in the amount of non-freezing water and freezing bound water and a decrease in free water. The number of water molecules entrapped in the curdlan jelly as non-freezing water was 8.1 per glucopyranose residue.


Subject(s)
Glucans/chemistry , Polysaccharides, Bacterial/chemistry , beta-Glucans , Calorimetry , Chemistry, Pharmaceutical , Delayed-Action Preparations , Humans , Suspensions , Theophylline/chemistry
SELECTION OF CITATIONS
SEARCH DETAIL
...