Sindhusha Vyshnavi B, Rajasekar Arvina
Periodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.
Cureus. 2024 Jul 1;16(7):e63631. doi: 10.7759/cureus.63631. eCollection 2024 Jul.
Background Herbs have been used in medical practice for centuries and continue to play a significant role in modern complementary and alternative medicine. Phytochemicals in these herbs possess strong antioxidant and anti-inflammatory properties, which are beneficial in targeting oral health issues, such as dental plaque, gingivitis, and oral microbial infections. As research progresses, the challenge remains to translate these natural compounds into safe, effective, and accessible treatments for a wide range of diseases. Aim The aim of this research was to formulate the neem and echinacea gel along with the evaluation of antimicrobial, anti-inflammatory, free-radical scavenging activity, and cytotoxic potential. Materials and methods The neem and echinacea gel was prepared using a concentrated powdered mixture of neem and echinacea (5 grams each) to which 100 ml of distilled water was added, and the mixture was boiled for 30 minutes at 60°C. The 10 ml concentrate was mixed with 20 ml of a carbopol and carboxymethyl cellulose (CMC) mixture and mixed thoroughly, which resulted in neem and echinacea gel. Then, the antimicrobial, anti-inflammatory, cytotoxic potential, and free-radical scavenging activity of the gel were evaluated. The data obtained were statistically analyzed with the help of a paired t-test, where a p-value of less than 0.05 was considered statistically significant. Results The antimicrobial assay showed that neem and echinacea gel at the concentration of 100 micrograms showed a greater zone of inhibition against S(3.15 ± 0.26), S (2.48 ± 0.45), E (2.89 ± 0.15), and (4.28 ± 0.87). The cytotoxic test revealed that even at an 80 µg concentration of the extract, more than 70% of the nauplii were vital, which indicated that the gel was not cytotoxic. The highest anti-inflammatory activity (78.39 ± 1.82) of the gel was seen at 50 micrograms when compared with diclofenac sodium (73.16 ± 1.80). The free radical scavenging activity showed that the 2,2-diphenyl-1-picrylhydrazyl (DPPH) absorbance of the neem and echinacea extract was highest at 50 micrograms. Conclusion The combination of neem and echinacea extract-based gel possessed high antimicrobial and anti-inflammatory activity when compared with standard drugs, such as amoxicillin and diclofenac sodium. The antioxidant activity of the gel was equal to butylated hydroxytoluene (BHT), and also the gel has a low cytotoxic potential even at its higher concentrations. Hence, the gel can be used as a natural remedy with minimal side effects, making it a valuable alternative to chemical agents.
背景
草药在医学实践中已使用了数百年,并且在现代补充医学和替代医学中继续发挥着重要作用。这些草药中的植物化学物质具有强大的抗氧化和抗炎特性,有助于解决口腔健康问题,如牙菌斑、牙龈炎和口腔微生物感染。随着研究的进展,将这些天然化合物转化为针对多种疾病的安全、有效且易于获取的治疗方法仍然是一项挑战。
目的
本研究的目的是制备印楝和紫锥菊凝胶,并评估其抗菌、抗炎、自由基清除活性和细胞毒性潜力。
材料和方法
将印楝和紫锥菊的浓缩粉末混合物(各5克)加入100毫升蒸馏水中,混合物在60°C下煮沸30分钟。将10毫升浓缩液与20毫升卡波姆和羧甲基纤维素(CMC)混合物充分混合,制成印楝和紫锥菊凝胶。然后,对该凝胶的抗菌、抗炎、细胞毒性潜力和自由基清除活性进行评估。所获得的数据借助配对t检验进行统计分析,p值小于0.05被认为具有统计学意义。
结果
抗菌试验表明,浓度为100微克的印楝和紫锥菊凝胶对金黄色葡萄球菌(抑菌圈直径为3.15±0.26)、表皮葡萄球菌(2.48±0.45)、大肠杆菌(2.89±0.15)和白色念珠菌(4.28±0.87)显示出更大的抑菌圈。细胞毒性试验表明,即使提取物浓度为80微克,超过70%的无节幼体仍存活,这表明该凝胶无细胞毒性。与双氯芬酸钠(73.16±1.80)相比,该凝胶在50微克时具有最高的抗炎活性(78.39±1.82)。自由基清除活性表明,印楝和紫锥菊提取物的2,2-二苯基-1-苦基肼(DPPH)吸光度在50微克时最高。
结论
与阿莫西林和双氯芬酸钠等标准药物相比,基于印楝和紫锥菊提取物的凝胶组合具有较高的抗菌和抗炎活性。该凝胶的抗氧化活性与丁基羟基甲苯(BHT)相当,并且即使在较高浓度下,该凝胶的细胞毒性潜力也较低。因此,该凝胶可作为副作用最小的天然药物使用,使其成为化学药剂的有价值替代品。