Buccal lidocaine mucoadhesive patches for pediatrics' teething pain: overcoming possible hazards of oral gels.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Development and Technology Pub Date : 2024-10-01 Epub Date: 2024-08-27 DOI:10.1080/10837450.2024.2393729
George Bebawy, Magda Samir Sokar, Ossama Y Abdallah
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Abstract

Objectives: The utilization of pharmaceutical products in pediatric medicine, while established for use in adults, often presents uncertainties due to differences in application for children. The FDA discourages the use of local anesthetic gels, notably lidocaine, for teething pain in pediatrics due to concerns regarding potential adverse effects if inadvertently swallowed excessively. Therefore, significant attention is being directed towards modifying available marketed products to make them suitable for pediatric use. Here, we introduce mucoadhesive patches that not only have an adjusted dose of lidocaine but also feature a controlled release profile to manage teething pain with prolonged effect. This design helps to prevent issues related to gel liquefaction and swallowing, thereby reducing the potential hazardous side effects of lidocaine in the pediatric population.

Methods: The study involved the development of controlled-release lidocaine HCl-loaded pellets forming a matrix for inclusion in mucoadhesive patches. Characterization was performed to ensure prolonged drug release, particularly during overnight use, aiming to improve pediatric patient compliance and enable precise dosing.

Key findings: The mucoadhesive patches exhibited sustained lidocaine release lasting 24 h, potentially offering overnight relief suitable for pediatric application. The analysis of lidocaine content revealed that the developed patches maintained stable levels compared to doses obtained from commercially available oral gels. This finding implies effective pain control without the need for frequent reapplications, alongside controlled doses that decrease the likelihood of side effects.

Conclusion: The formulated medicated patches demonstrated consistent lidocaine content, effectively controlled drug release, and consequently, reduced the likelihood of undesired side effects when compared to oral gel administration.

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治疗小儿出牙疼痛的颊用利多卡因粘胶贴剂:克服口服凝胶可能带来的危害。
目的:儿科用药中的药品虽然已确定用于成人,但由于在儿童应用中的差异,其使用往往存在不确定性。美国食品和药物管理局(FDA)不鼓励将局部麻醉凝胶(尤其是利多卡因)用于儿科出牙疼痛,因为人们担心,如果不慎吞服过量,可能会产生不良影响。因此,人们开始关注对市场上现有产品进行改良,使其适合儿科使用。在这里,我们介绍的粘液粘贴剂不仅具有可调整的利多卡因剂量,而且还具有控释特性,可长时间缓解出牙疼痛。这种设计有助于防止凝胶液化和吞咽等相关问题,从而减少利多卡因在儿科人群中的潜在危险副作用:该研究涉及开发可控释放的盐酸利多卡因颗粒,该颗粒形成一种基质,可用于粘液贴片。对其特性进行了分析,以确保药物的长期释放,尤其是在过夜使用期间,目的是提高儿科患者的依从性并实现精确给药:主要研究结果:粘胶贴片显示利多卡因的持续释放时间长达 24 小时,可提供适合儿科应用的过夜缓解。对利多卡因含量的分析表明,与市售口服凝胶的剂量相比,所开发的贴片能保持稳定的利多卡因含量。这一发现意味着无需频繁重复贴敷就能有效控制疼痛,同时还能控制剂量,降低出现副作用的可能性:结论:与口服凝胶相比,配制的药物贴片显示出稳定的利多卡因含量,有效控制了药物释放,从而降低了出现不良副作用的可能性。
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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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