Maria Mondéjar-López , María Paz García-Simarro , Julia Vega , Cristian Martínez Fajardo , Susana López-López , Oussama Ahrazem , Lourdes Gómez-Gómez , Felix L. Figueroa , Enrique Niza
{"title":"富含藏红花素的番茄提取物(Tomafran)的脂质体包封及其作为药妆成分的深入评价","authors":"Maria Mondéjar-López , María Paz García-Simarro , Julia Vega , Cristian Martínez Fajardo , Susana López-López , Oussama Ahrazem , Lourdes Gómez-Gómez , Felix L. Figueroa , Enrique Niza","doi":"10.1016/j.colsurfb.2025.114766","DOIUrl":null,"url":null,"abstract":"<div><div>This study evaluates the potential of a genetically modified, crocin-rich tomato extract (Tomafran) as a biological photoprotector and for skin health applications. Biochemical characterization and antioxidant capacity of Tomafran were assessed. Tomafran showed lower values than saffron in the ABTS assay, but similar values in the DPPH and BCBA assays. Additionally, Tomafran reduced advanced glycation end products (AGEs) and reactive oxygen species (ROS) in human fibroblasts, which are related to the negative effects of UV radiation on the skin. The extract was encapsulated in liposomes, yielding particles with an average size of 60.96 nm, a polydispersity index (PDI) of 0.06, a zeta potential of −21.50 mV, and a spherical morphology. The liposomal formulation demonstrated storage stability and a controlled release profile, with approximately 60 % of the extract released within the first 10 hours. The photoprotective capacity, measured through sun protection factor (SPF) and other biological protection factors, showed very slight improvements with increasing concentrations of Tomafran, achieving values lower than 2. The extract showed instability against UV radiation and high temperature, although encapsulation in liposomes provided protection. The anti-inflammatory properties of the liposomal Tomafran extract were evaluated using RAW 264.7 macrophage cells, showing significant reductions in proinflammatory interleukins IL-6 and IL-12. These findings highlight Tomafran's potential for mitigating inflammation associated with oxidative stress and UV-induced skin damage.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"253 ","pages":"Article 114766"},"PeriodicalIF":5.4000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Liposomal encapsulation of crocin-rich tomato extract (Tomafran) and its in-depth evaluation as a cosmeceutical ingredient\",\"authors\":\"Maria Mondéjar-López , María Paz García-Simarro , Julia Vega , Cristian Martínez Fajardo , Susana López-López , Oussama Ahrazem , Lourdes Gómez-Gómez , Felix L. Figueroa , Enrique Niza\",\"doi\":\"10.1016/j.colsurfb.2025.114766\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study evaluates the potential of a genetically modified, crocin-rich tomato extract (Tomafran) as a biological photoprotector and for skin health applications. Biochemical characterization and antioxidant capacity of Tomafran were assessed. Tomafran showed lower values than saffron in the ABTS assay, but similar values in the DPPH and BCBA assays. Additionally, Tomafran reduced advanced glycation end products (AGEs) and reactive oxygen species (ROS) in human fibroblasts, which are related to the negative effects of UV radiation on the skin. The extract was encapsulated in liposomes, yielding particles with an average size of 60.96 nm, a polydispersity index (PDI) of 0.06, a zeta potential of −21.50 mV, and a spherical morphology. The liposomal formulation demonstrated storage stability and a controlled release profile, with approximately 60 % of the extract released within the first 10 hours. The photoprotective capacity, measured through sun protection factor (SPF) and other biological protection factors, showed very slight improvements with increasing concentrations of Tomafran, achieving values lower than 2. The extract showed instability against UV radiation and high temperature, although encapsulation in liposomes provided protection. The anti-inflammatory properties of the liposomal Tomafran extract were evaluated using RAW 264.7 macrophage cells, showing significant reductions in proinflammatory interleukins IL-6 and IL-12. 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Liposomal encapsulation of crocin-rich tomato extract (Tomafran) and its in-depth evaluation as a cosmeceutical ingredient
This study evaluates the potential of a genetically modified, crocin-rich tomato extract (Tomafran) as a biological photoprotector and for skin health applications. Biochemical characterization and antioxidant capacity of Tomafran were assessed. Tomafran showed lower values than saffron in the ABTS assay, but similar values in the DPPH and BCBA assays. Additionally, Tomafran reduced advanced glycation end products (AGEs) and reactive oxygen species (ROS) in human fibroblasts, which are related to the negative effects of UV radiation on the skin. The extract was encapsulated in liposomes, yielding particles with an average size of 60.96 nm, a polydispersity index (PDI) of 0.06, a zeta potential of −21.50 mV, and a spherical morphology. The liposomal formulation demonstrated storage stability and a controlled release profile, with approximately 60 % of the extract released within the first 10 hours. The photoprotective capacity, measured through sun protection factor (SPF) and other biological protection factors, showed very slight improvements with increasing concentrations of Tomafran, achieving values lower than 2. The extract showed instability against UV radiation and high temperature, although encapsulation in liposomes provided protection. The anti-inflammatory properties of the liposomal Tomafran extract were evaluated using RAW 264.7 macrophage cells, showing significant reductions in proinflammatory interleukins IL-6 and IL-12. These findings highlight Tomafran's potential for mitigating inflammation associated with oxidative stress and UV-induced skin damage.
期刊介绍:
Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields.
Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication.
The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.