4.6 Article

Coffee silverskin: A possible valuable cosmetic ingredient

期刊

PHARMACEUTICAL BIOLOGY
卷 53, 期 3, 页码 386-394

出版社

TAYLOR & FRANCIS LTD
DOI: 10.3109/13880209.2014.922589

关键词

Agro-industrial by-products; antimicrobial activity; antioxidant activity; coffee industry residues; cosmetics; cytotoxicity; innovative revalorization of coffee by-products; skin care

资金

  1. Foundation for Science and Technology (Portugal) - POPH-QREN [SFRH/BDE/51385/2011]
  2. European Science Foundation
  3. COMPETE program [PEst-C/SAU/UI0709/2011]
  4. Fundação para a Ciência e a Tecnologia [SFRH/BDE/51385/2011] Funding Source: FCT

向作者/读者索取更多资源

Context: Currently, there is a great tendency in cosmetic area to use natural extracts. Coffee silverskin (CS) is the most abundant solid by-product generated during roasting of coffee processing. Objectives: To evaluate different CS extracts as promising cosmetic ingredients, regarding antioxidant, antimicrobial, and cytotoxic properties. Materials and methods: Aqueous, hydroalcoholic and ethanolic CS extracts were obtained by an environmentally friendly procedure considering costs and pollution. Extracts were characterized for total phenolic and flavonoid contents (TPC and TFC, respectively), antioxidant activity by 1,1-diphenyl-2-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP), antimicrobial activity expressed as minimal inhibitory concentration (MIC) and cytotoxicity using the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) and lactate dehydrogenase (LDH) assays in two skin cell lines (fibroblasts and keratinocytes). Results: The TPC of extracts was 18.33-35.25 mg of gallic acid equivalents per g of material on a dry basis (mg GAE/g db). The TFC of extracts was 1.08-2.47 mu g cathechin equivalents per g dry material (mu g CE/g db). The antioxidant activity was high, with values ranging between 95.95 and 216.40 mu mol Fe2+/g for aqueous and alcoholic samples, respectively. Preliminary assays for antimicrobial potential showed that extracts display antibacterial activity. The MIC varied from 31.3 to 250 mu g/mL for Gram-positive, and from 31.3 to 1000 mu g/mL for Gram-negative. Extracts did not affect in vitro cell viability, with values near 100% in all concentrations tested. Conclusion: Results seem show that CS is a safe source of natural antioxidants with antifungal and antibacterial activity and no cytotoxicity, with potential usefulness for cosmetic applications.

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