Eride Quarta, Fabio Sonvico, Ignazio La Mantia, Antonio Varricchio, Lucia Gloria, Massimiliano Minale, Niccola Funel, Francesca Buttini, Attilio Varricchio
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Six different APIs, used usually in Rhinopharynx pathology, were compared in order to investigate the dimension of MP emissions using four different devices. The results of a retrospective study including 74 subjects treated with standard therapy (ST) and the inhalation of nebulized Sobrerol (NS) were performed. Data regarding the persistence of clinical symptoms (i.e., cough and nasal constipation) were acquired. <b>Results:</b> No significant statistical differences among all the products tested (<i>p</i> > 0.05) were found. One device, Rinubes, demonstrated efficacy and robustness in the fine nebulization of all the pharmaceutical products analyzed. Rinubes delivered an aerosol cloud with significantly lower MMD (66.3 µm) than Mad Nasal and Spray-sol (142.1 and 116.0 µm, respectively), which would allow a higher fraction of drugs to be deposited in the retropharynx. 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引用次数: 0
摘要
背景/目的:可吸入微粒(IMPs)是目前侵入医学领域的一部分。事实上,鼻咽部的解剖区代表了许多不同病理和感染的温床,其中药物气溶胶微粒(MPs)的尺寸代表了治疗成功的判别因素。本工作的目的是证明一种新装置的功效及其气溶胶再现性在悬浮液的雾化沉积在咽后。材料与方法:采用低角度激光散射(LALLS)方法对MPs的尺寸和分布进行了评价。六种不同的api,通常用于鼻咽部病理学,为了调查使用四种不同的设备MP排放的尺寸进行比较。回顾性研究的结果包括74名接受标准治疗(ST)和雾化吸入Sobrerol (NS)的受试者。获得了有关临床症状(即咳嗽和鼻腔便秘)持续存在的数据。结果:各检测产品间差异无统计学意义(p < 0.05)。一种装置,Rinubes,在分析的所有药品的精细雾化中表现出有效性和稳健性。与Mad Nasal和Spray-sol(分别为142.1和116.0µm)相比,Rinubes提供的气溶胶云的MMD(66.3µm)明显更低,这将允许更高比例的药物沉积在咽后。回顾性临床研究显示,与对照组ST相比,NS治疗咳嗽缓解的几率更高(OR 9.18; p < 0.001),鼻症状缓解的几率更高(OR 6.7; p = 0.043)。结论:改进的可吸入MPs (INPAD)给药技术在克服控制药物在特定部位释放的生物学和解剖学障碍方面取得了重大进展。鼻咽疾病的挑战为非侵入性给药的发展提供了有希望的机会。
Site-Specific Microparticle Inhalation Therapy: A New Approach to Nasopharyngeal Symptoms.
Background/Objectives: Inhalable Microparticles (IMPs) are part of a currently invading field of medicine. In fact, the anatomical district of Rhinopharynx represents a bed for many different pathologies and infections, where the dimension of drug aerosol Microparticles (MPs) represents a discriminating factor to success therapy. The aims of the present work are to demonstrate the efficacy of a new device and its aerosol reproducibility in the nebulization of suspensions to be deposited in the retropharynx. Materials and Methods: The Low-Angle Laser Light Scattering (LALLS) method was used to evaluate both the dimension and distribution of MPs. Six different APIs, used usually in Rhinopharynx pathology, were compared in order to investigate the dimension of MP emissions using four different devices. The results of a retrospective study including 74 subjects treated with standard therapy (ST) and the inhalation of nebulized Sobrerol (NS) were performed. Data regarding the persistence of clinical symptoms (i.e., cough and nasal constipation) were acquired. Results: No significant statistical differences among all the products tested (p > 0.05) were found. One device, Rinubes, demonstrated efficacy and robustness in the fine nebulization of all the pharmaceutical products analyzed. Rinubes delivered an aerosol cloud with significantly lower MMD (66.3 µm) than Mad Nasal and Spray-sol (142.1 and 116.0 µm, respectively), which would allow a higher fraction of drugs to be deposited in the retropharynx. The retrospective clinical study revealed that NS treatment showed higher odds of cough resolution (OR 9.18; p < 0.001) with respect to control ST and showed higher odds of nasal symptom resolution (OR 6.7; p = 0.043). Conclusions: Improved techniques for the administration of inhalable MPs (INPAD) represent significant progress in overcoming the biological and the anatomical barriers in controlling drug release at a specific site. The challenges of nasopharyngeal pathologies offer promising opportunities for the development of non-invasive drug delivery.
PharmaceuticalsPharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍:
Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.