2016
DOI: 10.1016/j.ejpb.2016.02.009
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Application of Hansen Solubility Parameters to predict drug–nail interactions, which can assist the design of nail medicines

Abstract: We hypothesised that Hansen Solubility Parameters (HSPs) can be used to predict drug-nail affinities. Our aims were to: (i) determine the HSPs (δD, δP, δH) of the nail plate, the hoof membrane (a model for the nail plate), and of the drugs terbinafine HCl, amorolfine HCl, ciclopirox olamine and efinaconazole, by measuring their swelling/solubility in organic liquids, (ii) predict nail-drug interactions by comparing drug and nail HSPs, and (iii) evaluate the accuracy of these predictions using literature report… Show more

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Cited by 48 publications
(26 citation statements)
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“…Desired transdermal formulation should be site specific and effective. Even though, the rate of transportation is linked to the drug solubility and saturation in the carrier vehicle, more work need to be done to utilize and understand the fluidic nature of the formulation …”
Section: Introductionmentioning
confidence: 99%
“…Desired transdermal formulation should be site specific and effective. Even though, the rate of transportation is linked to the drug solubility and saturation in the carrier vehicle, more work need to be done to utilize and understand the fluidic nature of the formulation …”
Section: Introductionmentioning
confidence: 99%
“…Considering the plethora of drugs with unique physicochemical properties, a universal carrier for all the drugs seems impossible . There are various ways to assess the drug polymer compatibility which are thought to help to select a suitable carrier for a specific drug in time and cost effective manner. The extent of compatibility between MT and POx based carriers was calculated by the Hansen solubility parameter (HSP) ( Table 2 ).…”
Section: Resultsmentioning
confidence: 99%
“…The HSP approach within LBDDS has only been investigated to a limited extend, potentially due to the variability and complexity of the lipid excipient composition and the multitude of drug–excipient interactions. However, there are further pharmaceutical applications that are to some extent linked to lipids in general such as intestinal drug absorption, skin penetration of topically applied drugs, and prediction of drug–nail interactions . The available studies suggest that partial solubility parameters have the potential to be a useful tool in early development of LBDDS.…”
Section: Applications Of Solubility Parameters In Pharmaceuticsmentioning
confidence: 99%