2020
DOI: 10.1016/j.ijpharm.2020.119335
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Choline and amino acid based biocompatible ionic liquid mediated transdermal delivery of the sparingly soluble drug acyclovir

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Cited by 63 publications
(58 citation statements)
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“…Finally, the treated skins were processed according to our previous report [27] to estimate the topical drug delivery content (penetrated into the skin). The concentration of ACV was determined using HPLC with a Shiseido CAPCELL PAK C18 MG (4.6 mm × 250 mm) column using the United States Pharmacopeia (USP) method according to a previous report [28], where the mobile phase was 0.02 M glacial acetic acid with elution at a flow rate 1.5 mL/min, and the injected volume of sample was 100 µL. The concentration range of the standard curves was 0-25 µg/mL, and the squared correlation coefficient of the standard curve was more than 0.99 (R 2 > 0.99).…”
Section: Skin Permeation Studiesmentioning
confidence: 99%
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“…Finally, the treated skins were processed according to our previous report [27] to estimate the topical drug delivery content (penetrated into the skin). The concentration of ACV was determined using HPLC with a Shiseido CAPCELL PAK C18 MG (4.6 mm × 250 mm) column using the United States Pharmacopeia (USP) method according to a previous report [28], where the mobile phase was 0.02 M glacial acetic acid with elution at a flow rate 1.5 mL/min, and the injected volume of sample was 100 µL. The concentration range of the standard curves was 0-25 µg/mL, and the squared correlation coefficient of the standard curve was more than 0.99 (R 2 > 0.99).…”
Section: Skin Permeation Studiesmentioning
confidence: 99%
“…Nonetheless, ACV was solubilized state in IL, but as it is hydrophilic in nature, IL alone could not deliver ACV due to of the strong hydrophobic barrier functions of the skin [9]. On the other hand, though IPM, S/Comix/IPM, and W/O MEs disrupt the barrier function as they contain IPM, ACV could not permeate across the skin from these formulations because ACV was suspended in these systems, which probably obstructed the access of ACV to the skin [9,28].…”
Section: Skin Permeation Studiesmentioning
confidence: 99%
“…Work out of the same lab was not only able to improve upon the solubility of acyclovir using cholinium amino acid ILs but also allowed for transdermal delivery of the drug. [ 35 ] The use of ammonium and phosphonium chlorides showed enhancements of 60‐ to 120‐fold over aqueous solutions alone, and the use of imidazolium thiocyanate and dicyanamide demonstrated that both the cation and anion can operate synergistically to mediate interactions between the organic molecule and the aqueous solution, thus increasing the overall solubility. [ 36 ] Cholinium amino acid ILs were used to solubilize and stabilize paclitaxel, sterically and ionically, preventing the drug molecules from aggregating for 3 months.…”
Section: Biomedical Applicationsmentioning
confidence: 99%
“…Hence, Islam et al have recently reported the preparation of “ILs-in-oil” microemulsions (MEs) by combining hydrophilic choline-based ILs (“water”-like) with a mixture of the SAIL choline oleate and sorbitan laurate (“oil” phase), which allowed enhanced permeation of acyclovir through pig skin while showing no significant skin irritation [ 147 ]. The same authors have also investigated ternary systems comprising ethanol, isopropyl myristate, and choline/amino acid-based ILs, also with encouraging results for solubilization and skin permeation of acyclovir [ 148 ].…”
Section: Ionic Liquid-based Approaches In Dermal and Transdermal Drug Deliverymentioning
confidence: 99%