The changes to the chemical senses of taste and smell that accompany ageing are widely documented, and there has been some evidence that these changes may influence food preferences of the older consumer. However, little is known about the loss of function of the residual senses of texture and chemical irritant perception and how such losses influence food preferences. A consumer panel comprising a young (20–35 years) and an older (>65 years) age cohort was recruited and sensory tests were conducted to determine perceived intensity, preferences and the possibility of cross modal interaction between the sensory modalities of chemical irritation and texture. Liquid, semi-solid and solid food systems were studied to enable comparisons to be drawn. Older consumers were less capable of discriminating between chemical irritation and texture stimuli, indicating loss of sensory function, but there was indication that higher levels of chemical irritation were preferred among older consumers in some texture types. 相似文献
Context: The conventional liquid ophthalmic delivery systems exhibit short pre-corneal residence time and the relative impermeability to the cornea which leads to poor ocular bioavailability.
Objective: The aim of this study was to apply quality by design (QbD) for development of dexamethasone sodium phosphate (DSP) and tobramycin sulfate (TS)-loaded thermoresponsive ophthalmic in situ gel containing Poloxamer 407 and hydroxyl propyl methyl cellulose (HPMC) K4M for prolonging the pre-corneal residence time, ocular bioavability and decreases the frequency of administration of dosage form. The material attributes and the critical quality attributes (CQA) of the in situ gel were identified. Central composite design (CCD) was adopted to optimize the formulation.
Materials and methods: The ophthalmic in situ forming gels were prepared by cold method. Materials attributes were the amount of Poloxamer 407 and HPMC and CQA identified were Gel strength, mucoadhesive index, gelation temperature and % of drug release of both drug.
Results and discussion: Optimized batch (F*) containing 16.75% poloxamer 407 and 0.54% HPMC K4M were exhibited all results in acceptable limits. Compared with the marketed formulation, optimized in situ gel showed delayed Tmax, improved Cmax and AUC in rabbit aqueous humor, suggesting the sustained drug release and better corneal penetration and absorption.
Conclusion: According to the study, it could be concluded that DSP and TS would be successfully formulated as in situ gelling mucoadhesive system for the treatment of steroid responsive eye infections with the properties of sustained drug release, prolonged ocular retention and improved corneal penetration. 相似文献
Sodium laureth sulfate and amino acid type surfactants have been categorized as low‐skin irritation chemicals based on results of previous skin irritation tests. However, detergent‐induced skin irritation still occurs. Detergents with a low‐skin irritation effect are required, since the number of cosmetics for sensitive skin has increased. Therefore, an in vitro method of testing the safety of cosmetics for sensitive skin is required. Skin irritation by anionic surfactants was investigated to determine the effect of laureth‐3 carboxylate (polyoxyethylene lauryl carboxymethyl ether) amino acid salt on skin irritation. In addition, sodium laureth sulfate and amino acid type surfactants, regarded as low‐irritation surfactants, were also tested for skin irritation. The skin irritation effect of laureth‐3 carboxylate lysine salt (Surfactant 1 ), sodium laureth sulfate (Surfactant 2 ), and sodium N‐lauroyl glutamate (Surfactant 3 ) were investigated using a reconstructed human cultured epidermal model, LabCyte EPI‐MODEL24 6D. Cell viabilities of cultured epidermal cells exposed to Surfactant 1 (5.0 % aq.), Surfactant 2 , and Surfactant 3 were 82.0, 45.0 and 19.1 %, respectively. There were significant differences in cell viability upon exposure to 5.0 % aqueous test solutions of the three test chemicals. The results of the current investigation indicate that Surfactant 1 has a low skin‐irritation effect. 相似文献
Synopsis Few subjects are as problematical to dermatologists, cosmetologists and related experimenters involved in safety testing as the clinical assessment of skin colour. At the core of the problem is the word erythema, which does not communicate a sense for the nuance of red. In addition, light shades of red are not visible in dark-skinned people. Human assays aiming at evaluating the irritancy and allergic potential of cosmetics take advantage to use instrumental assessments of skin colour. However, there are pitfalls related to the complex biological aspects of the cutaneous reactivity, to the design of the in vivo assay, and to technical aspects bound to the principle of the measuring methods. Sound information can only be reached when these concerns are solved. Résumé Peu de sujets sont aussi problématiques pour les dermatologues, cosmétologues et autres expérimentateurs impliqués dans les tests de sûreté que l'évaluation clinique des couleurs cutanées. Au centre du problème est le mot érythème qui ne communique pas la notion des nuances de rouge. De plus, un érythème discret peut ne pas être visible chez des individus à la peau foncée. Les tests humains visant àévaluer les potentialités d'irritation et d'allergie aux cosmétiques bénéficient des évaluations instrumentales de la couleur cutanée. Cependant, il existe des pièges liés aux aspects biologiques complexes de la réactivité cutanée, au choix du test in vivo et à des aspects techniques en relation avec le principe du système de mesure. Une information adéquate ne peut être obtenue qu'après avoir résolu ces problèmes. 相似文献
Irritation potential of sodium laureth sulfate (SLES) alone, and in combination with lauryl glucoside (LG), polysorbate 20 (PS) and cocoamidopropyl betaine (CAPB) was tested in 13 human subjects. Four main and six sub-formulations were prepared and evaluated. Formulations were applied to the forearm as a 24 h close patch study. Irritation was scored by two different methods using an in vivo clinical protocol based on visual scoring and on the stratum corneum capacitance measurement. Irritation was found to be dose dependent. At 2 mg/patch level ten subjects did not show any skin reaction. At 20 mg/patch level eleven subjects showed a broad range of skin irritation. The highest irritation was observed with the formula that contained SLES, LG, and cocamide DEA together. Among the sub-formulations, cocamide DEA showed the highest irritation grade. A statistically significant correlation was observed between visual, clinical and corneometer scores. It was concluded that the irritation potential of surfactants was related to the total surfactant concentration, application mode, and the thermodynamic activity of molecules in the solution as well as the chemical structure of the surfactant molecules. 相似文献