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1.
Org Biomol Chem ; 19(8): 1752-1759, 2021 03 04.
Article En | MEDLINE | ID: mdl-33355577

Recently, sunscreen-based drug photocages have been introduced to provide UV protection to photoactive drugs, thus increasing their photosafety. Here, combined experimental and theoretical studies performed on a photocage based on the commercial UVA filter avobenzone (AB) and on the photosensitizing non-steroidal anti-inflammatory drug ketoprofen (KP) are presented unveiling the photophysical processes responsible for the light-triggered release. Particular attention is paid to solvent stabilization of the drug and UV filter excited states, respectively, which leads to a switching between the triplet excited state energies of the AB and KP units. Most notably, we show that the stabilization of the AB triplet excited state in ethanol solution is the key requirement for an efficient photouncaging. By contrast, in apolar solvents, in particular hexane, KP has the lowest triplet excited state, hence acting as an energy acceptor quenching the AB triplet manifold, thus inhibiting the desired photoreaction.


Anti-Inflammatory Agents, Non-Steroidal/chemistry , Ketoprofen/chemistry , Photosensitizing Agents/chemistry , Prodrugs/chemistry , Propiophenones/chemistry , Sunscreening Agents/chemistry , Anti-Inflammatory Agents, Non-Steroidal/radiation effects , Ethanol/chemistry , Hexanes/chemistry , Ketoprofen/radiation effects , Models, Chemical , Photolysis/radiation effects , Photosensitizing Agents/radiation effects , Prodrugs/radiation effects , Propiophenones/radiation effects , Solvents/chemistry , Sunscreening Agents/radiation effects , Ultraviolet Rays
2.
Anal Chim Acta ; 1093: 160-167, 2020 Jan 06.
Article En | MEDLINE | ID: mdl-31735210

In this study, poly(butyl methacrylate-co-ethyleneglycol dimethacrylate) polymeric monoliths were in situ developed within 0.75 mm i.d. poly(ethylene-co-tetrafluoroethylene) (ETFE) tubing by UV polymerization via three different free-radical initiators (α,α'-azobisisobutyronitrile (AIBN), 2,2-dimethoxy-2-phenylacetophenone (DMPA) and 2-methyl-4'-(methylthio)-2-morpholinopropiophenone (MTMPP). The influence of the nature of each photo-initiator and irradiation time on the morphological features of the polymer was investigated by scanning electron microscopy, and the chromatographic properties of the resulting microbore columns were evaluated using alkyl benzenes as test substances. The beds photo-initiated with MTMPP gave the best performance (minimum plate heights of 38 µm for alkyl benzenes) and exhibited a satisfactory reproducibility in the chromatographic parameters (RSD < 11%). These monolithic columns were also successfully applied to the separation of phenylurea herbicides, proteins and a tryptic digest of ß-casein.


Acetophenones/chemistry , Chromatography, High Pressure Liquid/instrumentation , Morpholines/chemistry , Nitriles/chemistry , Polymethacrylic Acids/chemistry , Polytetrafluoroethylene/analogs & derivatives , Propiophenones/chemistry , Acetophenones/radiation effects , Caseins/isolation & purification , Chromatography, High Pressure Liquid/methods , Herbicides/isolation & purification , Methacrylates/chemistry , Morpholines/radiation effects , Nitriles/radiation effects , Peptide Fragments/isolation & purification , Phenylurea Compounds/isolation & purification , Polymerization , Polymethacrylic Acids/chemical synthesis , Polytetrafluoroethylene/chemistry , Propiophenones/radiation effects , Ultraviolet Rays
3.
Eur J Pharm Sci ; 121: 309-318, 2018 08 30.
Article En | MEDLINE | ID: mdl-29874551

BACKGROUND: The growing incidence of photodamaging effects caused by UV radiation (e.g. sunburn, skin cancer) has increased the attention from health authorities which recommend the topical application of sunscreens to prevent these skin damages. The economic stakes for those companies involved in this international market are to develop new UV filters and innovative technologies to provide the most efficient, flexible and robust sunscreen products. Today the development of innovative and competitive sunscreen products is a complex formulation challenge. Indeed, the current sunscreens must protect against skin damages, while also being safe for the skin and being sensory and visually pleasant for the customers when applied on the skin. Organic UV filters, while proposing great advantages, also present the risk to penetrate the stratum corneum and diffuse into underlying structures with unknown consequences; moreover, their photo-stability are noted thorny outcomes in sunscreen development and subsequent performance. In recent years, the evaluation of the interaction between skin and sunscreen in terms of penetration after topical application has been considered from European authority but still its testing as their photo-stability assessment are not mandatory in most countries. OBJECTIVE: This study, based on in-vitro approaches, was performed to evaluate and compare the retention and the penetration of organic UV filters in free or encapsulated form inside the skin as well as their respective photo-stability. METHODS: Sunscreen formulation with a combination of Avobenzone and Octocrylene in "free form" and a formulation using the same UV filters but encapsulated in a sol-gel silica capsule, were analyzed and compared by FTIR Imaging Spectroscopy. Tape stripping method was used to investigate the penetration of these UV filters inside the stratum corneum. Their photo-stabilities were evaluated by spectroscopic measurements (FTIR, UV/Vis) and standard measurements were calculated: AUC (Area Under the Curve) and SPF (Sun Protection Factor). RESULT: With traditional formulation, the organic UV filters penetrated significantly into the stratum corneum while the same UV filters combined with encapsulation technology remained on the skin surface. The encapsulation technology also improved significantly their stability. CONCLUSION: Encapsulation technology is a promising strategy to improve the efficacy of sunscreen product using organic UV filters and to reduce safety problem. On the other hand, this study highlighted the pertinence of the FTIR Spectroscopy to test, compare and investigate sunscreen formulations.


Acrylates/administration & dosage , Propiophenones/administration & dosage , Sunscreening Agents/administration & dosage , Acrylates/chemistry , Acrylates/radiation effects , Animals , Drug Compounding , Drug Stability , Propiophenones/chemistry , Propiophenones/radiation effects , Skin/metabolism , Skin Absorption , Sunscreening Agents/chemistry , Sunscreening Agents/radiation effects , Swine , Ultraviolet Rays
4.
Chemphyschem ; 16(17): 3618-24, 2015 Dec 01.
Article En | MEDLINE | ID: mdl-26419334

The ultraviolet light component in the solar spectrum is known to cause several harmful effects, such as allergy, skin ageing, and skin cancer. Thus, current research attention has been paid to the design and fundamental understanding of sunscreen-based materials. One of the most abundantly used sunscreen molecules is Avobenzone (AB), which exhibits two tautomers. Here, we highlight the preparation of spherically shaped nanoparticles from the sunscreen molecule AB as well as from sunscreen-molecule-encapsulated polymer nanoparticles in aqueous media and study their fundamental photophysical properties by steady-state and time-resolved spectroscopy. Steady-state studies confirm that the AB molecule is in the keto and enol forms in tetrahydrofuran, whereas the enol form is stable in the case of both AB nanoparticles and AB-encapsulated poly(methyl methacrylate) (PMMA) nanoparticles. Thus, the keto-enol transformation of AB molecules is restricted to a nanoenvironment. An enhancement of photostability in both the nanoparticle and PMMA-encapsulated forms under UV light irradiation is observed. The efficient excited energy transfer (60 %) from AB to porphyrin molecules opens up further prospects in potential applications as light-harvesting systems.


Nanoparticles/chemistry , Photons , Polymethyl Methacrylate/chemistry , Propiophenones/chemistry , Propiophenones/radiation effects , Sunscreening Agents/chemistry , Sunscreening Agents/radiation effects , Nanoparticles/radiation effects , Polymethyl Methacrylate/radiation effects , Ultraviolet Rays
5.
Eur J Pharm Sci ; 78: 79-89, 2015 Oct 12.
Article En | MEDLINE | ID: mdl-26159738

Trans-resveratrol (RES) is used in cosmetic formulations and beta-carotene (BTC) is a classical sunscreen antioxidant, but their photostability in sunscreens, a property directly correlated to performance and safety has not been addressed in the literature. This paper reports the assessment of RES and/or BTC influence on the photostability of five UV-filters (octyl methoxycinnamate - OMC, avobenzone -AVO, octocrylene - OCT, bemotrizinole - BMZ, octyltriazone - OTZ) in three different combinations after UVA exposure followed by the identification of degradation products and the assessment of photoreactivity. The evaluation of sunscreen photostability was performed by HPLC and spectrophotometric analysis, and degradation products were identified by GC-MS analysis. Components RES, BTC, OMC and AVO were significantly degraded after UV exposure (reduction of around 16% in recovery). According to HPLC analysis, all formulations presented similar photostability profiles. Eleven degradation products were identified in GC-MS analysis, among them products of RES, BTC, OMC and AVO photodegradation. All evaluated formulations were considered photoreactive, as well as the isolated compounds RES and AVO. Considering HPLC, spectrophotometric and GC-MS results, it is suggested that formulations containing BMZ were considered the most photostable. The combination RES+BTC in a sunscreen improved the photostability of AVO. The benefits of using a combination of antioxidants in sunscreens was demonstrated by showing that using RES+BTC+studied UV-filters led to more photostable formulations, which in turn implies in better safety and efficacy.


Stilbenes/radiation effects , Sunscreening Agents/radiation effects , Ultraviolet Rays , beta Carotene/radiation effects , Acrylates/radiation effects , Benzoates/radiation effects , Chromatography, High Pressure Liquid , Cinnamates/radiation effects , Drug Stability , Gas Chromatography-Mass Spectrometry , Phenols/radiation effects , Photolysis , Propiophenones/radiation effects , Resveratrol , Singlet Oxygen/chemistry , Spectrophotometry, Ultraviolet , Superoxides/chemistry , Triazines/radiation effects
6.
Int J Pharm ; 492(1-2): 177-90, 2015 Aug 15.
Article En | MEDLINE | ID: mdl-26187167

Nail diseases are common, cause significant distress and treatments are far from successful. Our aim was to investigate the potential of UV-curable gels - currently used as cosmetics - as topical drug carriers for their treatment. These formulations have a long residence on the nail, which is expected to increase patient compliance and the success of topical therapy. The gels are composed of the diurethane dimethacrylate, ethyl methacrylate, 2-hydroxy-2-methylpropiophenone, an antifungal drug (amorolfine HCl or terbinafine HCl) and an organic liquid (ethanol or NMP) as drug solvent. Following its application to a substrate and exposure to a UVA lamp for 2 min, the gel polymerises and forms a smooth, glossy and amorphous film, with negligible levels of residual monomers. No drug-polymer interactions were found and drug loading did not affect the film's properties, such as thickness, crystallinity and transition temperatures. In contrast, the organic solvent did influence the film's properties; NMP-containing films had lower glass transition temperatures, adhesion and water resistance than ethanol-based ones. Water-resistance being a desired property, ethanol-based formulations were investigated further for stability, drug release and ungual permeation. The films were stable under accelerated stability testing conditions. Compared to terbinafine, amorolfine was released to a greater extent, had a higher ungual flux, but a lower concentration in the nailplate. However, both drugs were present at considerably high levels in the nail when their MICs are taken into account. We thus conclude that UV-curable gels are promising candidates as topical nail medicines.


Antifungal Agents/radiation effects , Drug Carriers/radiation effects , Ultraviolet Rays , Administration, Topical , Antifungal Agents/administration & dosage , Antifungal Agents/chemistry , Chemistry, Pharmaceutical , Drug Carriers/administration & dosage , Drug Carriers/chemistry , Drug Liberation , Ethanol/chemistry , Gels , Humans , Methacrylates/administration & dosage , Methacrylates/chemistry , Methacrylates/radiation effects , Methylmethacrylates/administration & dosage , Methylmethacrylates/chemistry , Methylmethacrylates/radiation effects , Morpholines/administration & dosage , Morpholines/chemistry , Morpholines/radiation effects , Nail Diseases/drug therapy , Nails/metabolism , Naphthalenes/administration & dosage , Naphthalenes/chemistry , Naphthalenes/radiation effects , Propiophenones/administration & dosage , Propiophenones/chemistry , Propiophenones/radiation effects , Pyrrolidinones/chemistry , Terbinafine , Urethane/administration & dosage , Urethane/analogs & derivatives , Urethane/chemistry , Urethane/radiation effects
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