Synthetic star shaped tetra-tailed biocompatible supramolecular amphiphile as an efficient nanocarrier for Amphotericin B

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Imdad Ali , Samiullah Burki , Jawad ur Rehman , Shafi Ullah , Ibrahim Javid , Magda H. Abdellattif , Muhammad Raza Shah
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引用次数: 1

Abstract

Macrocycle-based amphiphiles are capable of self-assembling into multidimensional nano-architecture with defined dimensions for various applications. Herein we report the synthesis, physio-chemical characterizations and oral drug delivery profiling of resorcinarene-based amphiphilic supramolecular macrocycle. The macrocycle was synthesized in two-step reaction and characterized using 1H NMR, Mass spectrometry and IR spectroscopic techniques. The synthesized macrocycle was assessed for vesicles formation, checked for biocompatibility and then Amphotericin B (Amp-B) was entrapped in macrocycle-based vesicles. The drug loaded vesicles were characterized for shape, size, homogeneity, drug entrapment, surface charge, in-vitro release profile and stability. Amp-B loaded macrocycle based vesicles were examined in rabbits for in-vivo bioavailability and compared with plan drug suspension. The synthesized macrocycle was non-toxic in normal mouse fibroblast cells, compatible with blood and safe in mice. The drug loaded macrocycle based vesicles appeared spherical with 279.4 nm size and − 12.2 mV zeta potential loading 85.45 % drug. The drug loaded vesicles storage stability for 30 days and gastric fluid stability for 1 h were it retained nearly 90 % drug at 30th day and 83.79 % drug at 1 h in gastric fluid. Oral bioavailability of Amp-B in rabbits was markedly enhanced when delivered in synthesized macrocycle based vesicles in comparison with plan drug suspension. Results of this study indicate that the synthesized star shaped tetra-tailed supramolecular amphiphile could be used as an efficient nanocarrier for enhancing oral bioavailability of drugs with solubility and bioavailability issues like Amp-B.

Abstract Image

合成星形四尾生物相容性超分子两亲体作为两性霉素B的高效纳米载体
基于大环的两亲体能够自组装成具有定义尺寸的多维纳米结构,用于各种应用。本文报道了间苯二甲酸二烯基两亲超分子大环的合成、理化性质和口服给药特性。采用两步法合成了该大环,并用1H NMR、质谱和红外光谱技术对其进行了表征。对合成的大环进行囊泡形成评价,检查生物相容性,然后将两性霉素B (Amphotericin B, Amp-B)包埋在大环囊泡中。对载药囊泡的形状、大小、均匀性、药物包裹、表面电荷、体外释放谱和稳定性进行表征。在家兔体内研究了负载Amp-B的大环囊泡的生物利用度,并与普通药物混悬液进行了比较。合成的大环对正常小鼠成纤维细胞无毒,与血液相容,对小鼠安全。载药大环囊泡呈球形,尺寸为279.4 nm, zeta电位为- 12.2 mV,载药率为85.45%。载药囊泡贮存稳定性为30 d,胃液贮存稳定性为1 h,第30天和第1 h胃液中药物残留率分别为近90%和83.79%。与普通药物混悬液相比,经合成大环囊泡给药可显著提高Amp-B在家兔体内的口服生物利用度。本研究结果表明,合成的星形四尾超分子两亲体可以作为一种有效的纳米载体,用于提高Amp-B等存在溶解度和生物利用度问题的药物的口服生物利用度。
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来源期刊
Chemistry and Physics of Lipids
Chemistry and Physics of Lipids 生物-生化与分子生物学
CiteScore
7.60
自引率
2.90%
发文量
50
审稿时长
40 days
期刊介绍: Chemistry and Physics of Lipids publishes research papers and review articles on chemical and physical aspects of lipids with primary emphasis on the relationship of these properties to biological functions and to biomedical applications. Accordingly, the journal covers: advances in synthetic and analytical lipid methodology; mass-spectrometry of lipids; chemical and physical characterisation of isolated structures; thermodynamics, phase behaviour, topology and dynamics of lipid assemblies; physicochemical studies into lipid-lipid and lipid-protein interactions in lipoproteins and in natural and model membranes; movement of lipids within, across and between membranes; intracellular lipid transfer; structure-function relationships and the nature of lipid-derived second messengers; chemical, physical and functional alterations of lipids induced by free radicals; enzymatic and non-enzymatic mechanisms of lipid peroxidation in cells, tissues, biofluids; oxidative lipidomics; and the role of lipids in the regulation of membrane-dependent biological processes.
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