Synthesis of calix (4) resorcinarene based amphiphilic macrocycle as an efficient nanocarrier for Amphotericin-B to enhance its oral bioavailability

IF 5.4 2区 医学 Q1 BIOPHYSICS
Imdad Ali , Amjad Ali , Li Guo , Samiullah Burki , Jawad Ur Rehman , Mahmood Fazal , Naushad Ahmad , Sarzamin Khan , Carlos A.T. Toloza , Muhammad Raza Shah
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引用次数: 0

Abstract

The supramolecular-based macrocyclic amphiphiles have fascinating attention and find extensive utilization in the pharmaceutical industry for efficient drug delivery. In this study, we designed and synthesized a new supramolecular amphiphilic macrocycle to serve as an efficient nanocarrier, achieved by treating 4-hydroxybenzaldehyde with 1-bromotetradecane. The derivatized product was subsequently treated with resorcinol to cyclize, resulting in the formation of a calix(4)-resorcinarene-based supramolecular amphiphilic macrocycle. The synthesized macrocycle and intermediate products were characterized using mass spectrometry, IR, and 1H NMR spectroscopic techniques. The amphotericin-B (Amph-B)-loaded and unloaded amphiphiles were screened for biocompatibility studies, vesicle formation, particle shape, size, surface charge, drug entrapment, in-vitro release profile, and stability through atomic force microscopy (AFM), Zetasizer, HPLC, and FT-IR. Amph-B -loaded macrocycle-based niosomal vesicles were investigated for in-vivo bioavailability in rabbits. The synthesized macrocycle exhibited no cytotoxicity against normal mouse fibroblast cells and was found to be hemocompatible and safe in mice following an acute toxicity study. The drug-loaded macrocycle-based vesicles appeared spherical, nano-sized, and homogeneous in size, with a notable negative surface charge. The vesicles remained stable after 30 days of storage. The results of Amph-B oral bioavailability and pharmacokinetics revealed that the newly tailored niosomal formulation enhanced drug solubility, protected drug degradation at gastric pH, facilitated sustained drug release at the specific target site, and delayed plasma drug clearance. Incorporating such advanced niosomal formulations in the field of drug delivery systems has the potential to revolutionize therapeutic outcomes and improve the quality of patient well-being.

Abstract Image

合成基于钙(4)间苯二酚的两亲大环,作为两性霉素-B 的高效纳米载体,提高其口服生物利用度
基于超分子的大环双亲化合物备受关注,并被广泛应用于医药行业的高效给药。在本研究中,我们设计并合成了一种新的超分子两亲大环,通过用 1-bromotetradecane 处理 4-hydroxybenzaldehyde 来作为高效纳米载体。衍生化产物随后经间苯二酚环化处理,形成了基于钙(4)-间苯二酚的超分子两亲大环。利用质谱、红外和 1H NMR 光谱技术对合成的大环和中间产物进行了表征。通过原子力显微镜(AFM)、Zetasizer、高效液相色谱和傅立叶变换红外光谱,对负载两性霉素-B(Amph-B)和未负载的两性化合物进行了生物相容性研究、囊泡形成、粒形、粒度、表面电荷、药物截留、体外释放曲线和稳定性筛选。研究人员在兔子体内研究了基于大环的 Amph-B 纳米囊泡的体内生物利用度。经过急性毒性研究发现,合成的大环对正常小鼠成纤维细胞没有细胞毒性,而且与血液相容,对小鼠安全。基于大环的载药囊泡呈球形、纳米级、大小均匀,表面带有明显的负电荷。囊泡储存 30 天后仍然保持稳定。Amph-B 的口服生物利用度和药代动力学研究结果表明,新定制的含膜配方提高了药物溶解度,保护了药物在胃 pH 值下的降解,促进了药物在特定靶点的持续释放,并延缓了血浆药物清除。在给药系统领域采用这种先进的尼索米尔制剂有可能彻底改变治疗效果,提高病人的生活质量。
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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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