Formulation and physicochemical characterization of azithromycin-loaded cubosomes.

IF 2.1 Q3 CHEMISTRY, MEDICINAL Research in Pharmaceutical Sciences Pub Date : 2023-02-01 DOI:10.4103/1735-5362.363595
Hoorieh Zaker, Somayeh Taymouri, Abolfazl Mostafavi
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Abstract

Background and purpose: Azithromycin (AZ) is a macrolide antibiotic that is soluble in saliva pH; its bitter taste can be well sensed, decreasing the ability of the patient to get the drug. Thus, handling such a bitter taste is challenging in developing the oral formulation. A wide range of methods has been applied to tackle this problem. Cubosomes are considered nanoparticles forming cubic three-dimensional structures with a taste-masking effect. This research aimed to apply cubosomes to mask AZ's bitter taste.

Experimental approach: Cubosomes which contained AZ were obtained by applying the film hydration method. Design expert software (version 11) was then employed for optimizing cubosomes that contained the drug. The encapsulation efficiency, particle size as well as polydispersity index of drug-loaded cubosomes were then subjected to evaluation. Assessment of particle morphology was done through SEM. The antimicrobial qualities of AZ-loaded cubosomes were then assessed by utilizing the disc diffusion method. Then, the taste masking study was carried out by referring to human volunteers.

Finding/results: AZ-loaded cubosomes were spherical in terms of shape and in the 166-272 nm range, with a polydispersity index of 0.17-0.33 and encapsulation efficiency of 80-92%. The results related to the microbial culture revealed that the antimicrobial qualities related to AZ-loaded cubosomes were like those of AZ. The results obtained by taste evaluation also revealed that the cubosomes could well mask the drug's bitter taste.

Conclusion and implications: These findings, thus, revealed that while the antimicrobial impact of AZ is not under the influence of loading in cubosomes, its taste could be well improved.

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载阿奇霉素立方体体的制备及理化性质研究。
背景与目的:阿奇霉素是一种可溶于唾液pH的大环内酯类抗生素;它的苦味可以被很好地感知,从而降低了患者获得药物的能力。因此,在开发口服配方时处理这种苦味是具有挑战性的。为了解决这个问题,已经采用了各种各样的方法。立方体被认为是纳米颗粒,形成立方体三维结构,具有味觉掩蔽效应。这项研究旨在利用立方体体来掩盖阿斯利康的苦味。实验方法:采用膜水化法制备含AZ的立方体体。然后使用设计专家软件(版本11)来优化含有该药物的立方体。并对载药立方体体的包封率、粒径及多分散指数进行了评价。通过扫描电镜对颗粒形貌进行了评估。然后用圆盘扩散法评价载az立方体体的抗菌性能。然后,通过参考人类志愿者进行味觉掩蔽研究。结果:负载az的立方体体呈球形,在166 ~ 272 nm范围内,多分散指数为0.17 ~ 0.33,包封率为80 ~ 92%。微生物培养结果表明,载AZ立方体体的抗菌性能与AZ相似。味觉评价结果也表明,立方体体可以很好地掩盖药物的苦味。结论与意义:上述研究结果表明,虽然AZ的抗菌作用不受立方体负载的影响,但其味道可以得到很好的改善。
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来源期刊
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences CHEMISTRY, MEDICINAL-
CiteScore
3.60
自引率
19.00%
发文量
50
审稿时长
34 weeks
期刊介绍: Research in Pharmaceutical Sciences (RPS) is included in Thomson Reuters ESCI Web of Science (searchable at WoS master journal list), indexed with PubMed and PubMed Central and abstracted in the Elsevier Bibliographic Databases. Databases include Scopus, EMBASE, EMCare, EMBiology and Elsevier BIOBASE. It is also indexed in several specialized databases including Scientific Information Database (SID), Google Scholar, Iran Medex, Magiran, Index Copernicus (IC) and Islamic World Science Citation Center (ISC).
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