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The Characteristics and Biological Activities of Niosome-Entrapped Salicylic Acid-Contained Oleoresin from for Skin Product Applications. | LitMetric

AI Article Synopsis

  • Salicylic acid (SA) is effective for skincare, particularly for treating acne and uneven skin texture, and a new formulation combining it with oleoresin from Yang-Na (ODA) was tested for its benefits.
  • The niosome formulation F4 improved the encapsulation and stability of SA and showed a sustained release pattern when combined with ODA, enhancing the absorption of the acid.
  • F4 also demonstrated the ability to reduce inflammation markers, suggesting it could be developed into an effective topical treatment for inflammatory skin conditions in the future.

Article Abstract

Salicylic acid (SA) is widely renowned for its efficacy as a beneficial ingredient for skincare, especially for acne and uneven skin texture. The salicylic acid (SA) niosome formulation combined with the essential component of oleoresin from Roxb. ex G. Don or Yang-Na (ODA) was developed and investigated for its physical characteristics, biological effects, and stability. The findings demonstrated that SA combined with ODA in the niosome formulation F4 enhanced the entrapment efficiency of SA, as well as the physical properties and stability of the formulation. Furthermore, the release pattern of this combined formulation indicated sustained release of SA. The permeation of SA was higher in the presence of ODA compared to SA-niosome formulations without ODA. Moreover, this F4 could downregulate the secretion of iNOS, COX-2, and TNF- including anti- activities. Consequently, the incorporation of ODA into the niosome formulation has the potential to improve the entrapment efficiency of SA, facilitating controlled release and enhancing permeation, nitric oxide inhibition capabilities, and anti activity. Therefore, F4 has the potential to be developed as a topical product for the combined treatment of inflammation and -associated conditions in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11442035PMC
http://dx.doi.org/10.1155/2024/1642653DOI Listing

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