Chaturvedi Kaushalendra, Shah Harsh S, Nahar Kajal, Dave Rutesh, Morris Kenneth R
Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, New York 11201, United States.
Division of Pharmaceutical Sciences, Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, New York 11201, United States.
ACS Omega. 2020 Apr 21;5(17):9690-9701. doi: 10.1021/acsomega.9b03886. eCollection 2020 May 5.
In the literature, it is reported that eutectics lead to the enhanced dissolution of a poorly soluble compound. However, the solubility theory suggests that since crystal structures of two components are unchanged that all else being equal, the dissolution rates of a fused mixture (FM) should be the same as a physical mixture (PM). The influence of crystal lattice energy on dissolution profiles was investigated using the PM and FM. Experimental phase diagrams constructed using differential scanning calorimetry data were compared with those theoretically derived. Deviation of the experimental phase diagram curves from the theoretical model indicates the nonideal behavior of both systems (ibuprofen/poly(ethylene glycol)-6000 and acetaminophen/caffeine). Both the binary systems showed an increase in the dissolution rate of the PM and FM. However, the dissolution from the PM was comparable with the FM's dissolution profile. The theoretical solubility calculations using the modified solubility equation showed that the use of the eutectic temperature instead of the drug's melting point should give a 3-4-fold increase in drug solubility. However, the correlation between dissolution and solubility calculation showed that the FM did not improve the dissolution when compared with the respective PM's dissolution profile. The proposed explanation is that the unchanged crystal lattice energy in eutectics still limits the solubility and therefore the dissolution rate.
在文献中,据报道低共熔物会导致难溶性化合物的溶出增强。然而,溶解度理论表明,由于两种组分的晶体结构不变,在其他条件均相同的情况下,熔融混合物(FM)的溶出速率应与物理混合物(PM)相同。使用物理混合物和熔融混合物研究了晶格能对溶出曲线的影响。将利用差示扫描量热法数据构建的实验相图与理论推导的相图进行了比较。实验相图曲线与理论模型的偏差表明这两种体系(布洛芬/聚乙二醇-6000和对乙酰氨基酚/咖啡因)均表现出非理想行为。这两种二元体系的物理混合物和熔融混合物的溶出速率均有所增加。然而,物理混合物的溶出与熔融混合物的溶出曲线相当。使用修正的溶解度方程进行的理论溶解度计算表明,用低共熔温度代替药物熔点可使药物溶解度提高3至4倍。然而,溶出与溶解度计算之间的相关性表明,与各自物理混合物的溶出曲线相比,熔融混合物并未改善溶出。提出的解释是,低共熔物中不变的晶格能仍然限制了溶解度,进而限制了溶出速率。