The Screening of Permeation Enhancers for Trans-Nail Delivery of Terbinafine Hydrochloride

A. Kushwaha
{"title":"The Screening of Permeation Enhancers for Trans-Nail Delivery of Terbinafine Hydrochloride","authors":"A. Kushwaha","doi":"10.4172/0975-0851.1000381","DOIUrl":null,"url":null,"abstract":"In this project, several permeation enhancers were screened to improve the penetration of terbinafine hydrochloride into the nail plate. Human nail plate clippings were used to perform the screening studies. As the results of high throughput screening, tween 80, tween 60, tween 40 and tween 20 showed the ability to improve the penetration of terbinafine into the nail clippings ~2.5, 2, 3 and 2.5-fold more compared to control. The amount of terbinafine penetrated in the nail clippings in case of PEG-35 castor oil and PEG-40 castor oil was ~2.5 and 2.5-fold more compared to control. Glycerol, sodium lauryl sulfate and span 80 enhanced the penetration of terbinafine into the nail clippings by ~2, 4.5 and 2.5-fold more compared to control. Transcutol, TPGS, propylene glycol, isopropyl myristate, octyldodecanol, decyl oleate and oleyl oleate were not able to improve the penetration of terbinafine in the nail clippings compare to control. Screening studies concluded that sodium lauryl sulfate was found to be potential permeation enhancer which improved the penetration of terbinafine significantly. *Corresponding author: Abhishek Singh Kushwaha, TranSkin Research Pvt. Ltd, Bhopal, Madhya Pradesh, India, Tel: +91 9981983734; E-mail: askushwaha@transkinresearch.com Received June 26, 2018; Accepted July 18, 2018; Published July 28, 2018 Citation: Kushwaha AS (2018) The Screening of Permeation Enhancers for TransNail Delivery of Terbinafine Hydrochloride. J Bioequiv Availab 10: 75-77. 381. doi: 10.4172/0975-0851.1000381 Copyright: © 2018 Kushwaha AS. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Permeation enhancers The total amount of terbinafine (μg/mg) Control 0.10 ± 0.03 Tween 80 0.26 ± 0.09 Glycerol 0.20 ± 0.07 Transcutol 0.18 ± 0.02 PEG-35 castor oil 0.25± 0.04 PEG-40 castor oil 0.25 ± 0.05 Sodium lauryl sulfate 0.45 ± 0.06 Tween 40 0.30 ± 0.03 Tween 20 0.25 ± 0.05 TPGS 0.14 ± 0.02 Tween 60 0.23 ± 0.03 Propylene glycol 0.12 ± 0.02 Span 80 0.25 ± 0.05 Isopropyl mystirate 0.08 ± 0.05 Octyl dodecanol 0.08 ± 0.01 Decyl oleate 0.08 ± 0.02 Oleyl oleate 0.10 ± 0.03 Table 1: The total amount of terbinafine extracted from the nail clippings. Citation: Kushwaha AS (2018) The Screening of Permeation Enhancers for Trans-Nail Delivery of Terbinafine Hydrochloride. J Bioequiv Availab 10: 75-77. 381. doi: 10.4172/0975-0851.1000381 J Bioequiv Availab, an open access journal ISSN: 0975-0851 Volume 10(3): 75-77 (2018) 76 Kimwipes®. Nail clipping was placed dipped in a testing formulation once and placed in a 5 ml glass vial. Glass vial was kept at room temperature. After 24 h, each nail clipping was washed 5 times with a 3 ml of 50% ethanol solution in water. Each nail clipping was pat dried with Kimwipes®. The amount of terbinafine is penetrated in the nail plate after 24 h was quantified using HPLC method [1,2,8]. Extraction of terbinafine from nail clipping: Before starting a terbinafine extraction procedure, the weight of each nail clipping was recorded and then each clipping was placed in a 5 ml glass vial which was filled with a 3 ml of DMSO to extract the terbinafine. Nail clipping in DMSO was shook for around 24 h. 1 ml of extraction sample was collected and then filtered to using 0.45 μm syringe filter. Extraction was analyzed using HPLC method [1,2,8]. Analytical method: The amount of terbinafine was quantified using Shimadzu Prominence-i 2030C plus HPLC (high-performance liquid chromatography) which was consisted of quaternary pump, auto sampler and UV-VIS Detector. The mobile phase was prepared by mixing aqueous phase and acetonitrile in a 60:40 proportion. The pH of the mobile was adjusted at pH 2 using 0.096M triethyl amine, 0.183M orthophosphoric acid. Terbinafine was eluted at a flow rate of 1.0 ml/min at 224 nm. The HPLC method was validated from 1 μg/ml of terbinafine to 10 μg/ml [9,10]. Statistical analysis: Statistical analysis of the data of high throughput screening studies was performed using ANOVA test. The p value less than 0.05 was considered statistical significant. Result and Discussion Nail plate consists of three layers which are dorsal, intermediate and ventral layer. Dorsal layer is the outer most layer which is considered to be the main barrier for the drug delivery [3]. Ventral layer is directly attached to the nail bed and it is more hydrated than dorsal layer. Topical nail delivery of drugs is mostly preferred for the treatment of nail diseases due to the direct application of drug on the site of infection. In recent years, many active (Iontophoresis, electroporation, and ultrasound) and passive (chemical penetration enhancers) techniques have been explored to improve the trans-ungual permeation the terbinafine [3,6,11]. Murthy et al., screened several permeation enhancers to improve the permeation of terbinafine across the nail [8]. Nair et al., also investigated the iontophoresis technique to improve the permeation of terbinafine [5]. Kushwaha et al. reported to deliver terbinafine hydrochloride from hyponychium region to the nail apparatus. In this project, we investigated some new permeations enhancers to enhance the penetration of terbinafine into the nail plate [12,13]. In topical formulations, permeation enhancers are chosen at the first-place due lower cost of treatment and patient compliance. Permeation enhancer are chemicals which improve the permeation of drugs into and across the nail plate using several mechanisms. Kushwaha et al. reported that some permeation enhancers break the disulfide bond of the keratin proteins and some improve the water holding capacity of nail plate to enhance the permeation of drugs into and across the nail plate [1,13]. In this project, vitamin ETPGS is used as a non-ionic surfactant. It is well known for its emulsifying and solubilizing the poor water-soluble drugs [14,15]. KolliphorTM RH 40 (PEG-40 castor oil) and Kolliphor® EL (PEG -35 castor oil) are commonly used as non-ionic solubilizer and emulsifier [15,16]. Tweens (Tween 20, 40, 60 and 80) and spans are non-ionic surfactant and used to as solubilizer and emulsifier [15]. Oleyl oleate, decyl oleate and octyldodecanol are used as the skin-Conditioning agent and permeation enhancers for skin delivery of drugs [17]. Isopropyl myristate is used as solvent and permeation enhancer for skin delivery of drugs [18]. Glycerol and propylene glycol are commonly used as moisturizing agent and solvents [15]. Transcutol is a very effective permeation enhancer and solvent for skin delivery of drugs. Sodium lauryl sulfate is a ionic surfactant, normally used in the shampoos and gels [2,15]. As a result of screening study, tween 80, tween 60, tween 40 and tween 20 improved the penetration of terbinafine ~2.5, 2, 3 and 2.5-fold more compared to control. The amount of terbinafine extracted from nail clippings in case of PEG-35 castor oil and PEG-40 castor oil was ~2.5 and 2.5-fold more compared to control. Glycerol, sodium lauryl sulfate and span 80 enhanced the penetration of terbinafine into the nail clippings by ~2, 4.5 and 2.5-fold more compared to control. Transcutol, TPGS, propylene glycol, isopropyl myristate, octyldodecanol, decyl oleate and oleyl oleate were not found to be effective to improve the penetration of terbinafine compare to control.","PeriodicalId":15184,"journal":{"name":"Journal of Bioequivalence & Bioavailability","volume":"10 1","pages":"1-3"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bioequivalence & Bioavailability","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/0975-0851.1000381","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

In this project, several permeation enhancers were screened to improve the penetration of terbinafine hydrochloride into the nail plate. Human nail plate clippings were used to perform the screening studies. As the results of high throughput screening, tween 80, tween 60, tween 40 and tween 20 showed the ability to improve the penetration of terbinafine into the nail clippings ~2.5, 2, 3 and 2.5-fold more compared to control. The amount of terbinafine penetrated in the nail clippings in case of PEG-35 castor oil and PEG-40 castor oil was ~2.5 and 2.5-fold more compared to control. Glycerol, sodium lauryl sulfate and span 80 enhanced the penetration of terbinafine into the nail clippings by ~2, 4.5 and 2.5-fold more compared to control. Transcutol, TPGS, propylene glycol, isopropyl myristate, octyldodecanol, decyl oleate and oleyl oleate were not able to improve the penetration of terbinafine in the nail clippings compare to control. Screening studies concluded that sodium lauryl sulfate was found to be potential permeation enhancer which improved the penetration of terbinafine significantly. *Corresponding author: Abhishek Singh Kushwaha, TranSkin Research Pvt. Ltd, Bhopal, Madhya Pradesh, India, Tel: +91 9981983734; E-mail: askushwaha@transkinresearch.com Received June 26, 2018; Accepted July 18, 2018; Published July 28, 2018 Citation: Kushwaha AS (2018) The Screening of Permeation Enhancers for TransNail Delivery of Terbinafine Hydrochloride. J Bioequiv Availab 10: 75-77. 381. doi: 10.4172/0975-0851.1000381 Copyright: © 2018 Kushwaha AS. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Permeation enhancers The total amount of terbinafine (μg/mg) Control 0.10 ± 0.03 Tween 80 0.26 ± 0.09 Glycerol 0.20 ± 0.07 Transcutol 0.18 ± 0.02 PEG-35 castor oil 0.25± 0.04 PEG-40 castor oil 0.25 ± 0.05 Sodium lauryl sulfate 0.45 ± 0.06 Tween 40 0.30 ± 0.03 Tween 20 0.25 ± 0.05 TPGS 0.14 ± 0.02 Tween 60 0.23 ± 0.03 Propylene glycol 0.12 ± 0.02 Span 80 0.25 ± 0.05 Isopropyl mystirate 0.08 ± 0.05 Octyl dodecanol 0.08 ± 0.01 Decyl oleate 0.08 ± 0.02 Oleyl oleate 0.10 ± 0.03 Table 1: The total amount of terbinafine extracted from the nail clippings. Citation: Kushwaha AS (2018) The Screening of Permeation Enhancers for Trans-Nail Delivery of Terbinafine Hydrochloride. J Bioequiv Availab 10: 75-77. 381. doi: 10.4172/0975-0851.1000381 J Bioequiv Availab, an open access journal ISSN: 0975-0851 Volume 10(3): 75-77 (2018) 76 Kimwipes®. Nail clipping was placed dipped in a testing formulation once and placed in a 5 ml glass vial. Glass vial was kept at room temperature. After 24 h, each nail clipping was washed 5 times with a 3 ml of 50% ethanol solution in water. Each nail clipping was pat dried with Kimwipes®. The amount of terbinafine is penetrated in the nail plate after 24 h was quantified using HPLC method [1,2,8]. Extraction of terbinafine from nail clipping: Before starting a terbinafine extraction procedure, the weight of each nail clipping was recorded and then each clipping was placed in a 5 ml glass vial which was filled with a 3 ml of DMSO to extract the terbinafine. Nail clipping in DMSO was shook for around 24 h. 1 ml of extraction sample was collected and then filtered to using 0.45 μm syringe filter. Extraction was analyzed using HPLC method [1,2,8]. Analytical method: The amount of terbinafine was quantified using Shimadzu Prominence-i 2030C plus HPLC (high-performance liquid chromatography) which was consisted of quaternary pump, auto sampler and UV-VIS Detector. The mobile phase was prepared by mixing aqueous phase and acetonitrile in a 60:40 proportion. The pH of the mobile was adjusted at pH 2 using 0.096M triethyl amine, 0.183M orthophosphoric acid. Terbinafine was eluted at a flow rate of 1.0 ml/min at 224 nm. The HPLC method was validated from 1 μg/ml of terbinafine to 10 μg/ml [9,10]. Statistical analysis: Statistical analysis of the data of high throughput screening studies was performed using ANOVA test. The p value less than 0.05 was considered statistical significant. Result and Discussion Nail plate consists of three layers which are dorsal, intermediate and ventral layer. Dorsal layer is the outer most layer which is considered to be the main barrier for the drug delivery [3]. Ventral layer is directly attached to the nail bed and it is more hydrated than dorsal layer. Topical nail delivery of drugs is mostly preferred for the treatment of nail diseases due to the direct application of drug on the site of infection. In recent years, many active (Iontophoresis, electroporation, and ultrasound) and passive (chemical penetration enhancers) techniques have been explored to improve the trans-ungual permeation the terbinafine [3,6,11]. Murthy et al., screened several permeation enhancers to improve the permeation of terbinafine across the nail [8]. Nair et al., also investigated the iontophoresis technique to improve the permeation of terbinafine [5]. Kushwaha et al. reported to deliver terbinafine hydrochloride from hyponychium region to the nail apparatus. In this project, we investigated some new permeations enhancers to enhance the penetration of terbinafine into the nail plate [12,13]. In topical formulations, permeation enhancers are chosen at the first-place due lower cost of treatment and patient compliance. Permeation enhancer are chemicals which improve the permeation of drugs into and across the nail plate using several mechanisms. Kushwaha et al. reported that some permeation enhancers break the disulfide bond of the keratin proteins and some improve the water holding capacity of nail plate to enhance the permeation of drugs into and across the nail plate [1,13]. In this project, vitamin ETPGS is used as a non-ionic surfactant. It is well known for its emulsifying and solubilizing the poor water-soluble drugs [14,15]. KolliphorTM RH 40 (PEG-40 castor oil) and Kolliphor® EL (PEG -35 castor oil) are commonly used as non-ionic solubilizer and emulsifier [15,16]. Tweens (Tween 20, 40, 60 and 80) and spans are non-ionic surfactant and used to as solubilizer and emulsifier [15]. Oleyl oleate, decyl oleate and octyldodecanol are used as the skin-Conditioning agent and permeation enhancers for skin delivery of drugs [17]. Isopropyl myristate is used as solvent and permeation enhancer for skin delivery of drugs [18]. Glycerol and propylene glycol are commonly used as moisturizing agent and solvents [15]. Transcutol is a very effective permeation enhancer and solvent for skin delivery of drugs. Sodium lauryl sulfate is a ionic surfactant, normally used in the shampoos and gels [2,15]. As a result of screening study, tween 80, tween 60, tween 40 and tween 20 improved the penetration of terbinafine ~2.5, 2, 3 and 2.5-fold more compared to control. The amount of terbinafine extracted from nail clippings in case of PEG-35 castor oil and PEG-40 castor oil was ~2.5 and 2.5-fold more compared to control. Glycerol, sodium lauryl sulfate and span 80 enhanced the penetration of terbinafine into the nail clippings by ~2, 4.5 and 2.5-fold more compared to control. Transcutol, TPGS, propylene glycol, isopropyl myristate, octyldodecanol, decyl oleate and oleyl oleate were not found to be effective to improve the penetration of terbinafine compare to control.
盐酸特比萘芬经甲给药促透剂的筛选
本课题筛选了几种渗透增强剂,以提高盐酸特比萘芬对甲板的渗透能力。人类指甲板剪报被用来进行筛选研究。高通量筛选结果显示,80、60、40和20处理的特比萘芬对指甲屑的穿透能力分别是对照的2.5倍、2倍、3倍和2.5倍。PEG-35蓖麻油组和PEG-40蓖麻油组的甲屑中特比萘芬的渗透量分别是对照组的2.5倍和2.5倍。甘油、十二烷基硫酸钠和span 80使特比萘芬对指甲屑的渗透比对照组提高了2倍、4.5倍和2.5倍。经甲醇、TPGS、丙二醇、肉豆酸异丙酯、辛基十二醇、癸基油酸酯和油酸油酯与对照相比,不能提高特比萘芬在指甲屑中的渗透性。筛选研究表明,十二烷基硫酸钠是潜在的渗透促进剂,可显著提高特比萘芬的渗透能力。*通讯作者:Abhishek Singh Kushwaha, TranSkin Research ppt . Ltd, Bhopal, Madhya Pradesh, India, Tel: +91 9981983734;邮箱:askushwaha@transkinresearch.com 2018年6月26日收稿;2018年7月18日录用;引用本文:Kushwaha AS(2018)盐酸特比萘芬经甲给药渗透增强剂的筛选。[J]中国生物医学工程学报(英文版),10(3):775 - 777。381. doi: 10.4172/0975-0851.1000381版权所有:©2018 Kushwaha AS。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。渗透增强剂的总量(μg /毫克)控制0.10±0.03渐变80 0.26±0.09甘油0.20±0.07 Transcutol 0.18±0.02 PEG-35蓖麻油0.25±0.04 PEG-40蓖麻油0.25±0.05十二烷基硫酸钠0.45±0.06渐变40 0.30±0.03渐变20 0.25±0.05 tpg 0.14±0.02渐变60 0.23±0.03丙二醇0.12±0.02跨越80年0.25±0.05异丙mystirate 0.08±0.05辛基十二烷醇0.08±0.01癸油酸0.08±0.02油酸油0.10±0.03表1:从指甲屑中提取的特比萘芬的总量。引用本文:Kushwaha AS(2018)盐酸特比萘芬经甲给药渗透促进剂的筛选。[J]中国生物医学工程学报(英文版),10(3):775 - 777。381. J Bioequiv Availab,开放获取期刊ISSN: 0975-0851 Volume 10(3): 75-77 (2018) 76 Kimwipes®。指甲钳在测试配方中蘸一次,放入5毫升玻璃瓶中。玻璃小瓶在室温下保存。24 h后,每个指甲盖用3ml 50%乙醇水溶液洗涤5次。每个指甲盖都用Kimwipes®轻轻拍干。24h后用高效液相色谱法定量特比萘芬在甲板中的渗透量[1,2,8]。从指甲夹中提取特比萘芬:在开始特比萘芬提取程序之前,记录每个指甲夹的重量,然后将每个指甲夹放入一个5ml的玻璃瓶中,玻璃瓶中装满3ml的DMSO以提取特比萘芬。将指甲夹在DMSO中摇匀约24 h,取提取样品1 ml,用0.45 μm注射器过滤。采用高效液相色谱法对提取物进行分析[1,2,8]。分析方法:采用岛津日珥-i 2030C加高效液相色谱法(高效液相色谱法),采用四元泵、自动进样器、紫外可见检测器组成。将水相与乙腈按60:40的比例混合制备流动相。用0.096M的三乙胺,0.183M的正磷酸,在pH为2的条件下调节移动液的pH。特比萘芬以1.0 ml/min的流速在224 nm洗脱。HPLC法在特比萘芬浓度为1 μg/ml至10 μg/ml范围内进行验证[9,10]。统计分析:采用方差分析对高通量筛选研究数据进行统计分析。p值小于0.05认为有统计学意义。结果与讨论甲板由背、中、腹三层组成。背层是最外层,被认为是药物传递的主要屏障。腹侧层与甲床直接相连,比背侧层含水量更高。由于药物直接应用于感染部位,局部给药是治疗指甲疾病的首选方法。近年来,人们探索了许多主动(离子电泳、电穿孔和超声)和被动(化学渗透增强剂)技术来提高特比萘芬的跨爪渗透[3,6,11]。Murthy等人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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