High-stability compound chlorhexidine iodohydrin solution and preparation method thereof
A compound chlorhexidine iodine, high-stable technology, which can be used in pharmaceutical formulations, active ingredients of iodine compounds, and medical preparations of non-active ingredients, etc., can solve the problems of iodine loss, easy generation of drug-resistant bacteria, and increased synthesis cost. , to achieve the effect of reducing iodine loss, ingenious design and fast onset
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0034] 1.3 Preparation of highly stable compound chlorhexidine iodine alcohol solution
[0035] Add 0.1-2 parts by weight of 10% PVPI, 0.1-1 parts by weight of chlorhexidine acetate and 0.01-0.23 parts by weight of iodine into a three-necked flask containing 50-70 parts by weight of ethanol, and simultaneously add 0.01-0.3 parts by weight of KI , stirring and reacting for about 2-3 hours at 40-60° C. under sealed conditions, and then adding 0.1-2 parts by weight of surfactant and humectant and 29.36-42.69 parts by weight of water after cooling. Finally, adjust the pH to 2-4 with phosphoric acid.
[0036] 1.4 Determination of available iodine content
[0037] The available iodine concentration of the sample can be determined with reference to the potentiometric titration method in the Chinese Pharmacopoeia [2] method. In this experiment, the potentiometric titration method in the Chinese Pharmacopoeia was used to measure the effective iodine content: accurately pipette 25ml o...
Embodiment 1
[0080] Add 0.1 parts by weight of 10% PVPI, 0.1 parts by weight of chlorhexidine acetate and 0.23 parts by weight of iodine into a three-necked flask filled with 70 parts by weight of ethanol, and add 0.01 parts by weight of KI at the same time, and stir the reaction at 40°C under sealed conditions for 3 About hour, just add the tensio-active agent (0.01 weight part K30 of 0.09 weight part OB-2 and the humectant glycerin of 0.1 weight part after cooling, and the water of 29.36 weight parts respectively after cooling. Regulate pH with phosphoric acid at last to be 2 .
[0081] After testing, the sample was prepared according to the disinfection technical specifications and the requirements of the Chinese Pharmacopoeia. The available iodine was 0.19%. After the stability test was accelerated for 14 days, the degradation rate was 6.11%. It was applied on the arm, and the arm was dry after 2-3 minutes. No obvious yellowing phenomenon, easy to wash off with water. The average kill...
Embodiment 2
[0086] Add 1 part by weight of 10% PVPI, 0.51 parts by weight of chlorhexidine acetate and 0.13 parts by weight of iodine into a three-necked flask filled with 60 parts by weight of ethanol, and add 0.15 parts by weight of KI at the same time, and stir the reaction at 50 °C under sealed conditions for 2.5 About hours, after cooling, 1 part by weight of surfactant NP-10, 1 part by weight of humectant K30, and 36.21 parts by weight of water were added respectively. Finally, the pH was adjusted to 3 with phosphoric acid.
[0087] After testing, the sample was prepared according to the disinfection technical specifications and the requirements of the Chinese Pharmacopoeia. The available iodine was 0.2%. After the stability test was accelerated for 14 days, the degradation rate was 3.11%. It was applied on the arm, and the arm was dry after 2-3 minutes. No obvious yellowing phenomenon, easy to wash off with water. In the microbial sterilization test, the average kill log value of ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com