2008
DOI: 10.1208/s12249-008-9162-5
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Penetration and Distribution of Thiocolchicoside through Human Skin: Comparison Between a Commercial Foam (Miotens® ) and a Drug Solution

Abstract: Abstract. Penetration and distribution of thiocolchicoside from a commercially available foam (Miotens ® 0.25%, w/v) through human excised full-thickness skin were evaluated using two different in vitro apparatus: a Franz diffusion cell and a Saarbruecken penetration model-based cell. In order to evaluate the intrinsic capability of the drug to penetrate into the skin, a simple drug aqueous solution prepared at the same drug concentration as Miotens ® was also tested. Results showed that both apparatus were su… Show more

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Cited by 20 publications
(9 citation statements)
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“…TCC transdermal delivery, which has been studied by Artusi et al [ 20 ] , has the advantage of avoiding systemic side effects and improving patient compliance. In the form of nongreasy topical foams or gels, particularly when associated to skin penetration enhancers, [ 21 , 22 ] TCC may represent a well tolerated and effective formulation for the treatment and prevention of muscle contractures.…”
Section: Introductionmentioning
confidence: 99%
“…TCC transdermal delivery, which has been studied by Artusi et al [ 20 ] , has the advantage of avoiding systemic side effects and improving patient compliance. In the form of nongreasy topical foams or gels, particularly when associated to skin penetration enhancers, [ 21 , 22 ] TCC may represent a well tolerated and effective formulation for the treatment and prevention of muscle contractures.…”
Section: Introductionmentioning
confidence: 99%
“…In the case presented here, the results of patch tests on intact skin (negative in immediate reading) and open tests (positive only on inflamed skin) may indicate that epicutaneously applied TCD can induce an immediate reaction only when a damaged epidermal barrier is present. This finding is not surprising, considering the physicochemical properties of TCD-in particular its relatively high molecular weight of 563 daltons-which are not favorable to the drug permeating easily and rapidly through skin, as shown by Aguzzi et al on human excised full-thickness skin specimens (6). In the study by Aguzzi et al (6), in fact, TCD cutaneous amounts were very low or almost absent within the first hour of incubating the skin samples with TCD-containing products, including a 0.25% drug aqueous solution.…”
Section: Discussionmentioning
confidence: 83%
“…This finding is not surprising, considering the physicochemical properties of TCD-in particular its relatively high molecular weight of 563 daltons-which are not favorable to the drug permeating easily and rapidly through skin, as shown by Aguzzi et al on human excised full-thickness skin specimens (6). In the study by Aguzzi et al (6), in fact, TCD cutaneous amounts were very low or almost absent within the first hour of incubating the skin samples with TCD-containing products, including a 0.25% drug aqueous solution. Higher drug quantities were found after increasing the incubation time by using the same simple aqueous solution utilized for skin tests in the case presented here.…”
Section: Discussionmentioning
confidence: 83%
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“…A significant difference in the epidermal thickness was observed between the two protocols (p<0.05) (Supplementary Figure S8). Epidermal thickness increase likely results from tissue over-hydration that results from the dermis being in constant contact with the aqueous media reservoir in the Franz cell for 24 hrs [4751]. CLSM results showed a higher presence of QDs in the mouse skin at the end of 6 and 24 hours using the petri dish exposure protocol compared to the Franz diffusion cell (Figure 6).…”
Section: Resultsmentioning
confidence: 99%