Use of rhamnose and derivatives thereof as antifungal agents
Through the combination of rhamnose-rich polysaccharides and other antifungal agents, the existing problems of high recurrence rate and drug resistance in the treatment of seborrheic dermatitis are solved, an efficient and safe antifungal effect is achieved, and the growth of Malassezia is significantly inhibited. growth and reduces the risk of drug toxicity.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0074] A cream having the composition shown in the table below was prepared according to a method comprising the following steps:
[0075] 1. Combine Phase A ingredients in the order given, stirring after each addition, until a homogeneous bulk phase is obtained. The bulk phase is then heated to 75°C to 80°C.
[0076] 2. Weigh phase B ingredients, heat to 75°C to 80°C and mix until a homogeneous phase is obtained.
[0077] 3. When the temperature of both phases is between 75°C and 80°C, slowly add phase B to phase A, then homogenize the mixture.
[0078] 4. Cool the mixture obtained in step 3 to 55°C, adjust the pH with sodium hydroxide and add the other ingredients of phase C in the order given, stirring after each addition until a homogeneous bulk phase is obtained.
[0079] 5. Cool the mixture obtained in step 4 to 20°C to 30°C.
[0080]
Embodiment 2 and comparative example 3
[0082] A cream with the composition shown in the table below was prepared according to the method described in Example 1.
[0083]
[0084] Antifungal Activity Test
[0085] Human organotypic skin cultures were obtained from abdominal skin removed during plastic surgery. These skin explants were altered by partial removal of the stratum corneum to facilitate colonization, and MF suspensions were placed on the skin surface and incubated for 24 h under conditions optimal for MF growth. 24 hours after the initial MF inoculation, NSFC was topically applied to the skin explants (2 mg / cm 2 ) and spread evenly. On control skin explants inoculated in the same manner, no product was applied (C2). The sham control group was treated with petrolatum, a neutral cream with no known antifungal properties (P3). MF growth was monitored by quantifying MF colony forming units (CFU) in samples removed from the skin surface. CFUs were quantified by recovering fungal microorganisms from s...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More