高稀释度的药物在电子光谱上表现出明显的差异

N. Sukul, Sumit Ghosh, R. Singh, N. Pande, A. Sukul
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引用次数: 1

摘要

高稀释药物对人、动物和植物都有治疗作用。实验证据表明,自由水分子和OH基团的氢键强度构成了hd的物理基础,否则将缺乏原始药物分子。HDs是通过在每一步机械搅拌或搅拌的情况下连续稀释一种物质而在水溶液中产生的,称为效价。本研究使用了两种药物(NaCl)及其母酊剂(MT)的6、12、30 cH三种效价。在190 nm ~ 350 nm波长范围内,测定了90% EtOH的MTs和电位的电子能谱。目的是找出除上述两个因素外,效力中任何额外的物理化学实体。据报道,电荷转移(CT)相互作用伴随着药物的增强。本研究的重点是CT相互作用。结果表明,测试样品的光谱模式和吸光度强度各不相同。增强包括连续电位的CT相互作用。水和EtOH不形成均匀的混合物,有EtOH和水分子的聚集体。CT相互作用发生在这些单独的聚集体中,并且主要发生在EtOH或水中的分子间。这些聚合体在测试样本中彼此不同。结果表明,水和EtOH聚集体及其相对分布构成了附加的植物化学基础。
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High Dilutions of Drugs show Distinct Variation from each other in their Electronic Spectra
Drugs at high dilution (HD) produce therapeutic effect on man, animals and plants. Experimental evidence shows that free water molecules and hydrogen bond strength of OH groups constitute the physical basis of HDs which are otherwise devoid of original drugs molecules. HDs are produced in aqueous EtOH   by serial dilution of a substance with mechanical agitation or succussion in each step, and are called potencies. Three potencies 6 cH, 12 cH and 30 cH of two drugs Anacardium orientale and Natrum muriaticum (NaCl) and their mother tincture (MT) are used in this study. Electronic spectra of these MTs and potencies, all in 90% EtOH, were taken in the wavelength region of 190 nm – 350 nm. The objective is to find out any additional physico-chemical entities in potencies besides the aforesaid two factors. It was reported earlier that charge transfer (CT) interaction accompanies potentization of drugs. This study focused on the CT interaction. The results indicate that spectral pattern and absorbance intensities of the test samples vary from each other. Potentization involves CT interaction in consecutive potencies. Water and EtOH do not form a homogeneous mixture and have aggregates of EtOH and water molecules. CT interactions occur in these individual aggregates and are mostly inter molecular within EtOH or water. These aggregates vary from each other in the test samples. It is concluded that water and EtOH aggregates and their relative distribution constitute additional phyco-chemical basis of potencies.
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