Department of Pharmaceutical Sciences, Lovely Professional University, Jalandhar-Delhi, G.T. Road (NH-1), Phagwara, Jalandhar, Punjab, India, 144411.
AAPS PharmSciTech. 2016 Jun;17(3):700-9. doi: 10.1208/s12249-015-0401-2. Epub 2015 Aug 28.
The objectives of the current investigation are (1) to prepare and characterize (particle size, surface charge (potential zeta), surface morphology by transmission electron microscopy, drug content, and drug release) the azithromycin (AZM, 100 mg)-loaded oil-in-water (o/w) macroemulsion, (2) to assess the toxicity of macroemulsion with or without AZM using RBC lysis test in comparison with AZM in phosphate buffer solution of pH 7.4, (3) to compare the in vitro antimicrobial activity (in Escherichia coli using zone inhibition assay) of AZM-loaded macroemulsion with its aqueous solution, and (4) to assess the in vitro anti-inflammatory effect (using egg albumin denaturation bioassay) of the AZM-loaded macroemulsion in comparison with diclofenac sodium in phosphate buffer solution of pH 7.4. The AZM-loaded macroemulsion possessed the dispersed oil droplets with a mean diameter value of 52.40 ± 1.55 μm. A reversal in the zeta potential value from negative (-2.16 ± 0.75 mV) to positive (+6.52 ± 0.96 mV) was noticed when AZM was added into the macroemulsion. At a 1:5 dilution ratio, 2.06 ± 0.03 mg of drug was released from macroemulsion followed by 1.01 ± 0.01 and 0.25 ± 0.08 mg, respectively, for 1:10 and 1:40 dilution ratios. Antimicrobial activity maintenance and significant reduction of RBC lysis property were noticed for AZM after loaded in the macroemulsion. However, an increment in the absorbance values for emulsion-treated samples in comparison to the control samples was noticed in the anti-inflammatory test. This speculates the potential of the AZM-loaded emulsion to manage inflammatory conditions produced at Acne vulgaris.
(1)制备并表征阿奇霉素(AZM,100mg)载药油包水乳状液(o/w 型)的(粒径、表面电荷(Zeta 电位)、表面形态(透射电子显微镜观察)、药物含量和药物释放);(2)与 AZM 在 pH7.4 的磷酸盐缓冲液中的毒性进行比较,用红细胞溶血试验评估载药乳状液及其无载药乳状液的毒性;(3)比较 AZM 载药乳状液及其水溶液在体外的抗菌活性(大肠杆菌抑菌圈试验);(4)与 pH7.4 的磷酸盐缓冲液中的扶他林钠相比,评估 AZM 载药乳状液的体外抗炎效果(卵白蛋白变性生物测定)。AZM 载药乳状液的分散油滴平均粒径为 52.40±1.55μm。当 AZM 加入乳状液中时,Zeta 电位值从负(-2.16±0.75mV)变为正(+6.52±0.96mV)。在 1:5 的稀释比例下,乳状液中释放了 2.06±0.03mg 的药物,随后分别在 1:10 和 1:40 的稀释比例下释放了 1.01±0.01mg 和 0.25±0.08mg 的药物。AZM 载入乳状液后,抗菌活性得以维持,且红细胞溶血性质显著降低。然而,在抗炎试验中,与对照样品相比,乳状液处理的样品的吸光度值增加。这推测了 AZM 载乳剂在治疗寻常痤疮引起的炎症条件方面的潜力。