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Improvised strategy of ethanolic nanovesicular gel of phospholipon 90G for transdermal delivery of luliconazole to mitigate fungal diseases

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Abstract

The research work involves the development and characterization of ethanolic nanovesicular gel of different concentrations of the specified chemicals so as to estimate the optimized one among the rest. For the determination of its stability and suitability, optimized formulation was carried to a number of evaluation parameters such as particle size, zeta potential, polydispersity index (PDI), % entrapment efficiency (%EE), attenuated total internal reflection Fourier transforms infra-red spectroscopy (ATR-FTIR), transmission electron microscopy (TEM), atomic force microscopy (AFM), in vitro drug permeation study, stability studies, viscosity, pH, spreadability, extrudability, and last but not least, anti-fungal activity done by considering tube dilution assay. And finally, the results obtained were recorded and analyzed for all the parameters. The outcomes revealed that among nine nanovesicular formulations, ENV5 was found to be optimized, as because of its appropriate results for particle size, PDI, and zeta potential and highest % entrapment efficiency of about 169.5 nm, 0.407, −37.9 mV, and 80.07 ± 0.55% respectively, whereas in vitro drug permeation study expresses % cumulative release of 78.59 ± 0.43 in about 24 h. The suspension of nanovesicular system and lyophilized form of nanovesicular suspension both were examined and found to be very much stable at 4°C/60 ± 5 % RH than that of 25 °C/60 ± 5 % RH. Ultimately, the outcomes of the evaluation parameters have proved that the buildup is stable and suitable for topical application hence, leading to efficacious therapy of fungal diseases.

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References

  1. Sutton CL, Taylor ZE, Farone MB, Handy ST (2017) Antifungal activity of substituted aurones. Bioorg. Med. Chem. Lett. 27:901–903. https://doi.org/10.1016/j.bmcl.2017.01.012

    Article  Google Scholar 

  2. Dave V, Kumar D, Lewis S, Paliwal S (2010) Ethosome for enhanced transdermal drug delivery of aceclofenac. Int. J. Drug Deliv. 2:81–92. https://doi.org/10.5138/ijdd.2010.0975.0215.02016

    Article  Google Scholar 

  3. Dave V, Yadav RB, Kushwaha K (2017) Herbal liposome for the topical delivery of ketoconazole for the effective treatment of seborrheic dermatitis. J. Microencapsul. 21:67–77. https://doi.org/10.1007/s13204-017-0634-3

    Article  Google Scholar 

  4. Dave V, Gupta A, Singh P, Tak K, Sharma S (2019) PEGylated Lipova E120 liposomes loaded with celecoxib: in-vitro characterization and enhanced in-vivo anti-inflammatory effects in rat models. J. Biosci. 44:82–94. https://doi.org/10.1007/s12038-019-9919-x

    Article  Google Scholar 

  5. Sheehan DJ, Hitchcock CA, Sibley CM (1999) Current and emerging azole antifungal agents. Clin Microbiol Rev. 12:40–79. https://doi.org/10.1128/CMR.12.1.40

    Article  Google Scholar 

  6. Kim HS, Song IH, Kim JC (2006) In vitro and in vivo gene transferring characteristics of novel cationic lipids, DMKD (O, O 0-dimyristyl-N-lysyl aspartate) and DMKE (O, O0-dimyristyl-N-lysylglutamate). J. Control Release. 11:234–241. https://doi.org/10.1016/j.jconrel.2006.08.003

    Article  Google Scholar 

  7. Kanwal Q, Hussain I, Siddiqui HL, Javaid A (2010) Antifungal activity of flavonoids isolated from mango (Mangifera indica L.) leaves. Natural Product Research. 24(20):1907–1914. https://doi.org/10.1080/14786419.2010.488628

    Article  Google Scholar 

  8. Ling G, Zhang P, Zhang W, Sun J, Meng Z, Qin Y, Deng Y, He Z (2010) Development of novel self-assembled DS-PLGA hybrid nanoparticles for improving oral bioavailability of vincristine sulphate by P-gp inhibition. J. Control Release. 148:241–248. https://doi.org/10.1016/j.jconrel.2010.08.010

    Article  Google Scholar 

  9. Ainbinder D, Protokin R, Chaouat M, Touitou E (2009) Effect of honokiol and 5-FU on non-melanoma skin cancer cells. J. Drug Del. Sci. Tech. 19:283–287. https://doi.org/10.1016/S1773-2247(09)50053-6

    Article  Google Scholar 

  10. Panigrahi L, Ghosal SK, Pattnaik S, Maharana L, Barik BB (2006) Effect of permeation enhancers on the release and permeation kinetics of lincomycin hydrochloride gel formulations through mouse skin Indian J. Pharm. Sci. 68:205–211. https://doi.org/10.4103/0250-474X.25716

    Article  Google Scholar 

  11. Pathana IB, Jawarea BP, Shelkeb S, Ambekarc W (2017) Curcumin loaded ethosomes for transdermal application: formulation, optimization, in-vitro and in-vivo study. J Drug Deliv Sci Technol. 44:49–57. https://doi.org/10.2174/1567201815666171207163010

    Article  Google Scholar 

  12. Ahmad N, Ahmad R, Al-Qudaihi A, Alaseel SE, Fita IZ, Khalid MS, Bolla SR (2019) A novel self-nanoemulsifying drug delivery system for curcumin used in the treatment of wound healing and inflammation. 3. Biotech. 9(10):1–20. https://doi.org/10.1007/s13205-019-1885-3

    Article  Google Scholar 

  13. Hallan SS, Sguizzato M, Mariani P, Cortesi R, Huang N, Simelière F, Esposito E (2020) Design and characterization of ethosomes for transdermal delivery of caffeic acid. Pharmaceutics 12(8):1–19 pharmaceutics12080740

    Article  Google Scholar 

  14. Touitou E, Dayan N, Bergelson L, Godin B, Eliaz M (2000) Ethosomes-novel vesicular carriers for enhanced delivery: characterization and skin penetration properties. J Control Release. 65(3):403–418. https://doi.org/10.1016/s0168-3659(99)00222-9

    Article  Google Scholar 

  15. Godin B, Touitou E (2003) Ethosomes: new prospects in transdermal delivery. Crit Rev Ther Drug Carrier Syst 20(1):63–102. https://doi.org/10.1615/critrevtherdrugcarriersyst.v20.i1.20

    Article  Google Scholar 

  16. Dayan N, Touitou E (2000) Carriers for skin delivery of trihexyphenidyl HCl: ethosomes vs. liposomes. Biomaterials 21(18):1879–1885. https://doi.org/10.1016/s0142-9612(00)00063-6

    Article  Google Scholar 

  17. Jain S, Tiwary AK, Sapra B, Jain NK (2007) Formulation and evaluation of ethosomes for transdermal delivery of lamivudine. AAPS Pharm Sci Tech 8(4):249–257. https://doi.org/10.1208/pt0804111

    Article  Google Scholar 

  18. Yang L, Wu L, Wu D, Shi D, Wang T, Zhu X (2017) Mechanism of transdermal permeation promotion of lipophilic drugs by ethosomes. Int J Nanomedicine 12:3357–3364. https://doi.org/10.2147/ijn.s134708

    Article  Google Scholar 

  19. Riaz M, Riaz M, Zhang X, Lin C, Wong K, Chen X, Yang Z (2018) Surface functionalization and targeting strategies of liposomes in solid tumor therapy: a review. Int. J. Mol. Sci. 19(1):1–27. https://doi.org/10.3390/ijms19010195

    Article  Google Scholar 

  20. Sguizzato M, Mariani P, Spinozzi F, Benedusi M, Cervellati F, Cortesi R, Esposito E (2020) Ethosomes for coenzyme Q10 cutaneous administration: from design to 3D skin tissue evaluation. Antioxidants. 9(6):1–19. https://doi.org/10.3390/antiox9060485

    Article  Google Scholar 

  21. Giulimondi F, Digiacomo L, Pozzi D, Palchetti S, Vulpis E, Capriotti AL, Caracciolo G (2019) Interplay of protein corona and immune cells controls blood residency of liposomes. Nat. Commun. 10(1):1–11. https://doi.org/10.1038/s41467-019-11642-

    Article  Google Scholar 

  22. Chen Z J, Yang S C, Liu X L, Gao Y, Dong X, Lai X, Fang C. (2020). Nanobowl-supported liposomes improve drug loading and delivery. Nano Lett https://doi.org/10.1021/acs.nanolett.0c00495

  23. Pathan IB, Jaware BP, Shelke S, Ambekar W (2018) Curcumin loaded ethosomes for transdermal application: formulation, optimization, in-vitro and in-vivo study. J Drug Deliv Sci Technol. 44:49–57. https://doi.org/10.1016/j.jddst.2017.11.005

    Article  Google Scholar 

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Correspondence to Prashansa Sharma.

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Dave, V., Gupta, N., Prakesh, A. et al. Improvised strategy of ethanolic nanovesicular gel of phospholipon 90G for transdermal delivery of luliconazole to mitigate fungal diseases. Biomass Conv. Bioref. 13, 15463–15469 (2023). https://doi.org/10.1007/s13399-021-02039-y

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