鞘氨醇精油的植物化学特征和协同抗菌作用,作为现代抗生素的辅助剂对抗耐药性

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S489517
Zifang Shang, Vipasha Sharma, Tarun Kumar, Kamal Dev, Sandip Patil
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引用次数: 0

摘要

背景:多重耐药菌对全球的威胁严重限制了有效抗生素的选择。本研究重点关注 C. oppositifolia 提取物的抗菌活性和植物化学特征,旨在发现新型植物治疗药物:C.oppositifolia标本-叶和花序。标本经清洗、消毒、干燥和研磨成细粉。用索氏提取器提取甲醇和石油醚,然后用氯仿、正丁醇和乙酸乙酯进行分馏。使用 Clevenger 仪器通过水蒸馏提取挥发油。进行植物化学分析以确定生物活性化合物。生物物理技术包括紫外-可见分光光度法、TLC、HPLC、GC-MS、傅立叶变换红外光谱和 NMR,用于表征。采用琼脂井法和圆盘扩散法测试了金黄色葡萄球菌 ATCC25922 和大肠杆菌 ATCC25922 的抗菌活性,并评估了与红霉素和阿莫西林的协同作用:甲醇提取物具有抑菌活性,对金黄色葡萄球菌和大肠杆菌的抑菌区均为 13.0 ± 0.2 毫米。石油醚、氯仿、正丁醇和乙酸乙酯馏分显示出不同的抑菌区。红霉素具有杀菌活性,当与甲醇提取物和挥发油结合使用时,红霉素的杀菌活性会协同增强,从而增加对金黄色葡萄球菌的抑制区。植物化学分析确定了酚类、黄酮类、单宁、香豆素、生物碱、萜类、皂苷和苷类。傅立叶变换红外光谱分析发现了胺、醛、腈、烯和砜等官能团。气相色谱-质谱(GC-MS)鉴定出 24 种化合物,其中α-蒎烯、叶黄素和蒈烯是主要成分。核磁共振光谱显示,油和抗生素之间没有形成复合物,这表明这些化合物起到了增效作用:结论:C. oppositifolia 提取物具有显著的抗菌活性和增效潜力,尤其是对金黄色葡萄球菌。各种生物活性化合物的存在表明,它们在开发基于植物的新疗法方面大有可为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phytochemical Characterization and Synergistic Antibacterial Effects of Colebrookea Oppositifolia Essential Oil as Adjuvants to Modern Antibiotics in Combating Drug Resistance.

Background: The global threat of multi-drug-resistant bacteria has severely limited the options available for effective antibiotics. This study focuses on the antimicrobial activity and phytochemical characterization of C. oppositifolia extracts, aiming to identify novel plant-based therapeutic agents.

Methods: C. oppositifolia specimens-leaves and inflorescence. Specimens were cleaned, sterilized, dried, and ground into a fine powder. Extracts were obtained using methanol and petroleum ether via a Soxhlet apparatus, followed by fractionation with chloroform, n-butanol, and ethyl acetate. Volatile oil was extracted through hydro distillation using a Clevenger apparatus. Phytochemical analysis was conducted to identify bioactive compounds. Biophysical techniques, including UV-visible spectrophotometry, TLC, HPLC, GC-MS, FTIR, and NMR, were employed for characterization. Antimicrobial activity was tested against S. aureus ATCC25922 and E. coli ATCC25922 using agar well and disc diffusion methods, and synergistic effects were assessed with erythromycin and amoxicillin.

Results: Methanol extract exhibited bacteriostatic activity with inhibition zones of 13.0 ± 0.2 mm for both S. aureus and E. coli. Petroleum ether, chloroform, n-butanol, and ethyl acetate fractions showed varying inhibition zones. Erythromycin demonstrated bactericidal activity, which was enhanced synergistically when combined with methanol extract and volatile oil, increasing inhibition zones against S. aureus. Phytochemical analysis identified phenols, flavonoids, tannins, coumarins, alkaloids, terpenoids, saponins, and glycosides. FTIR analysis revealed functional groups such as amines, aldehydes, nitriles, alkenes, and sulfones. GC-MS identified 24 compounds, with α-pinene, caryophyllene, and carene as major components. NMR spectra indicated no complex formation between oils and antibiotics, suggesting the compounds act as synergists.

Conclusion: The C. oppositifolia extracts possess significant antimicrobial activity and synergistic potential, particularly against S. aureus. The presence of various bioactive compounds suggests a promising role in developing new plant-based therapeutics.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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