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1.
Int J Cosmet Sci ; 42(6): 529-535, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32895982

ABSTRACT

This work analyses the role of proteoglycans on skin ageing, influenced by the presence of glycosylated proteins, which exercise diverse functions on the skin. They are essential components that restore the cells, providing hydration, maintaining hydration of the extracellular matrix, preventing the formation of wrinkles thanks to their ability to combine to other molecules such as collagen or hyaluronic acid and favouring the smoothness of the skin texture. The use of these proteins is a very recent and promising topic, since their application may revolutionize skin ageing therapies. Of the existing proteoglycans, decorin, versican and perlecan are of special note, playing a fundamental role on skin.


Nous avons analysé dans cette étude le rôle des protéoglycanes dans le vieillissement de la peau, conditionné par la présence des protéines glycosylées qui exercent plusieurs fonctions sur la peau. Ce sont des composants essentiels qui restaurent les cellules, fournissent de l'hydratation en maintenant l'hydratation de la matrice extracellulaire en évitant la formation de rides cutanées grâce à sa capacité de se combiner à d'autres molécules tels que le collagène ou l'acide hyaluronique qui favorisent la douceur de la peau. L'utilisation de ces protéines est un des sujets les plus récents et prometteurs, étant donné que son application peut représenter une révolution quant aux thérapies qui luttent contre le vieillissement cutané. Parmi les protéoglycanes ressortent la décorine, le versicane et le perlécane qui jouent un rôle fondamental sur le derme.


Subject(s)
Proteoglycans/physiology , Skin Aging/physiology , Humans
2.
Drug Deliv ; 22(6): 869-76, 2015.
Article in English | MEDLINE | ID: mdl-24670096

ABSTRACT

Tricyclic antidepressants, as doxepin hydrochloride (DH), may have analgesic local effect due to its biochemical mechanism of action. Delivery of DH directly to the oral cavity could be an interesting alternative for toothache due to its analgesic local effect. One problem associated with the mucosal administration routes is the short residence time of the dosage form on the mucosal membranes. In this sense, we have developed new doxepin mucoadhesive films able of reducing pain and increasing the effectiveness of treatment. For this purpose, we tested three different polymers: chitosan, sodium hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (SCMC) in film elaboration. The results obtained show that all films are hydrophilic matrices that absorb water when placed in an aqueous media. All the films hydrated very quickly, reaching high percentage of swelling after just few minutes (5 min for SCMC, 2 min for HPMC and 30 min for chitosan). Moreover, the SCMC and HPMC films were dissolved whereas chitosan was not dissolved. Dissolution also leads to viscous liquids with a higher retention time over mucosal surfaces what may lead to adhesive interactions. In vitro permeation studies showed that for all the formulations studied, SCMC (19.91%), HPMC (69.5%) and chitosan (24.17%), the percentage of drug permeated increased compared to the drug solution (8.26%). Specifically the HPMC film presents greater amounts of doxepin permeated (49.27 ± 4.47 µg/cm(2)).


Subject(s)
Antidepressive Agents, Tricyclic/administration & dosage , Carboxymethylcellulose Sodium/chemistry , Chitosan/chemistry , Doxepin/administration & dosage , Hypromellose Derivatives/chemistry , Toothache/drug therapy , Adhesiveness , Administration, Buccal , Calorimetry, Differential Scanning , Chemistry, Pharmaceutical , Drug Liberation , Hydrogen-Ion Concentration
3.
Int J Pharm ; 467(1-2): 84-9, 2014 Jun 05.
Article in English | MEDLINE | ID: mdl-24699354

ABSTRACT

Fast dissolving disintegrating tablets (FDDTs) containing different dosages of melatonin have been manufactured for administration to a specific target population: pediatric patients, having potential difficulties taking other oral forms. The lower dosages (3 and 5mg) are intended for epileptic children, migraine prevention, neurodevelopmental disability, sleep disorders and blindness. Dosages of 10 and 60 mg are intended for Duchenne muscular dystrophy. Two FDDT groups have been designed, one which has excipients for direct compression and others having direct compression and effervescent excipients. Tablets have been produced having disintegration times of less than 25s and with friability and hardness values that require no special storage or packaging conditions.


Subject(s)
Melatonin/chemistry , Chemistry, Pharmaceutical , Excipients/chemistry , Hardness , Hardness Tests , Kinetics , Solubility , Tablets , Technology, Pharmaceutical/methods
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