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Potential combination topical therapy of anal fissure: development evaluation and clinical study†

机译:潜在的局部联合肛裂治疗:发展评估和临床研究†

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摘要

To treat anal fissure, internal anal sphincterotomy may be associated with surgical risks and incidence of incontinence. Botulinum toxin injection into the anal sphincter is invasive and expensive. Headache and hypotension hindered topical treatment with glyceryl trinitrate. Greater patient compliance, potentiated efficacy, reduced side effects, and lower cost are the major advantages offered by the combination therapy. Therefore, combination topical gels of nifedipine (NIF), lidocaine hydrochloride (LDH) and betamethasone valerate (BMV) were prepared and evaluated regarding viscosity, pH, drug content, and in vitro release. Compatibility study of drug–drug and drug-excipient mixtures preceded the formulation. Stability study was performed. A prospective randomized clinical trial was conducted for six weeks to assess the efficacy of the optimized formula in the treatment of anal fissure either acute (AAF, 37 patients) or chronic (CAF, 34 patients) in comparison with three single drug market products. The compatibility was indicated except in case of LDH with each of poloxamer 407 (P407), methylparaben, and propylparaben as well as BMV with P407. The gels showed acceptable viscosity ranges, tolerated pH values, and drugs content limits complying with the pharmacopeial limit. The gel containing 10% Transcutol® (F2) was selected as optimized formula due to the significant (p < 0.05) enhancement in NIF release. The recommended storage temperature was 8 °C. In comparison with the market products, the optimized gel can be represented as a potential combination therapy of acute and chronic anal fissures as suggested by significantly increased healing% and significantly reduced pain, bleeding, anal discharge and itching without side effects.
机译:为了治疗肛裂,肛门内括约肌切开术可能与手术风险和失禁的发生率有关。向肛门括约肌注射肉毒杆菌毒素是侵入性的并且昂贵。头痛和低血压阻碍了三硝酸甘油酯的局部治疗。更大的患者依从性,增强的疗效,减少的副作用和更低的成本是联合疗法提供的主要优势。因此,制备了硝苯地平(NIF),盐酸利多卡因(LDH)和戊酸倍他米松(BMV)的局部组合凝胶,并评估了其粘度,pH,药物含量和体外释放。药物-药物和药物-赋形剂混合物的相容性研究先于制剂。进行稳定性研究。进行了为期六周的前瞻性随机临床试验,以评估与三个单一药物市场产品相比,优化配方在治疗急性(AAF,37例患者)或慢性(CAF,34例)肛门裂中的疗效。指出了相容性,但在LDH与泊洛沙姆407(P407),对羟基苯甲酸甲酯和对羟基苯甲酸丙酯以及BMV与P407的情况下除外。凝胶显示出可接受的粘度范围,容许的pH值和符合药典限制的药物含量限制。选择含有10%Transcutol®(s2)(F2)的凝胶作为优化配方,因为NIF释放显着(p <0.05)增强。推荐的存储温度为8°C。与市售产品相比,经过优化的凝胶可以代表急性和慢性肛裂的潜在组合疗法,这可以通过显着提高治愈率并显着减少疼痛,出血,肛门分泌物和瘙痒而无副作用来表明。

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