Van Wassenhoven Michel, Goyens Martine, Henry Marc, Capieaux Etienne, Devos Philippe
Federal Agency for Medicines and Health Products, Homeopathic Medicines Commission, Brussels, Belgium.
Pharmaceutical Association for Homeopathy, Wépion, Belgium.
Homeopathy. 2017 Nov;106(4):223-239. doi: 10.1016/j.homp.2017.08.001. Epub 2017 Sep 28.
NMR proton relaxation is sensitive to the dynamics of the water molecule HO, through the interaction of the spin of the proton (H) with external magnetic and electromagnetic fields.
We measured dilution and potentization processes through measurements of H spin-lattice T and spin-spin T relaxation times. In order to interpret the recorded fluctuations in T- or T-values, experimental data were linearized by investigating how the area under a fluctuating time = f(dilution) curve (dilution integral or DI) changes with dilution. Two kinds of fitting procedures were considered: chi-square fitting with a goodness-of-fit probability, and least absolute deviations criterion with Pearson's linear correlation coefficient.
We showed that fluctuations are not attributable to random noise and/or experimental errors, evidencing a memory effect quantifiable by the slope of the DI = f(dilution) straight line. For all experiments, correlation coefficients were found to lie above 0.9999, against 0.999 for random noise. The discrimination between experimental slopes and slopes associated with random noise data was very good at a five-sigma level of confidence (i.e. probability 3 × 10). Discrimination between experimental slopes at a five-sigma level was possible in most cases, with three exceptions: gelsemium aqua pura v gelsemium dilution (four-sigma); copper aqua pura v gelsemium aqua pura (four-sigma) and copper simple dilution v gelsemium simple dilution (three-sigma). All potentized samples show very good discrimination (at least nine-sigma level) against aqua pura, lactose or simple dilution. It was possible to transform the associated relaxation times into a molecular rotational correlation time τ and an average spin-spin distance d. Our experiments thus point to a considerable slowing down of molecular movements (τ > 1300 ps or T = 224-225 K) around water molecules up to a distance of 3.7 Å, values. It was also possible to rule out other possible mechanisms of relaxation (diffusive motion, O-H relaxation or coupling with the electronic spin, S = 1, of dissolved dioxygen molecules).
There is clear evidence that homeopathic solutions cannot be considered as pure water as commonly assumed. Instead, we have evidenced a clear memory effect upon dilution/potentization of a substance (water, lactose, copper, gelsemium) reflected by different rotational correlation times and average H⋯H distances. A possible explanation for such a memory effect may lie in the formation of mesoscopic water structures around nanoparticles and/or nanobubbles mediated by zero-point fluctuations of the vacuum electromagnetic field as suggested by quantum field theories. The existence of an Avogadro's 'wall' for homeopathically-prepared medicines is not supported by our data. Rather it appears that all dilutions have a specific material configuration determined by the potentized substance, also by the chemical nature of the containers, and dissolved gases and the electromagnetic environment. This sensitivity of homeopathically-prepared medicines to electromagnetic fields may be amplified by the highly non-linear processing routinely applied in the preparation of homeopathic medicines. Future work is needed in such directions. The time is now ripe for a demystification of the preparation of homeopathic remedies.
核磁共振质子弛豫通过质子(H)自旋与外部磁场和电磁场的相互作用,对水分子HO的动力学敏感。
我们通过测量H自旋晶格T和自旋 - 自旋T弛豫时间来测量稀释和增效过程。为了解释记录的T或T值波动,通过研究波动时间=f(稀释)曲线下的面积(稀释积分或DI)如何随稀释变化,将实验数据线性化。考虑了两种拟合程序:具有拟合优度概率的卡方拟合,以及具有皮尔逊线性相关系数的最小绝对偏差准则。
我们表明波动并非归因于随机噪声和/或实验误差,证明了一种可通过DI = f(稀释)直线斜率量化的记忆效应。对于所有实验,发现相关系数高于0.9999,而随机噪声的相关系数为0.999。在五西格玛置信水平(即概率3×10)下,实验斜率与随机噪声数据相关斜率之间的区分非常好。在大多数情况下,在五西格玛水平下区分实验斜率是可能的,有三个例外:纯水钩吻素稀释(四西格玛);纯铜溶液对纯水钩吻素溶液(四西格玛)和铜简单稀释对钩吻素简单稀释(三西格玛)。所有增效样品与纯水、乳糖或简单稀释相比,显示出非常好的区分(至少九西格玛水平)。可以将相关的弛豫时间转换为分子旋转相关时间τ和平均自旋 - 自旋距离d。因此,我们的实验表明,在距离水分子高达3.7Å的范围内,分子运动(τ>1300 ps或T = 224 - 225 K)明显减慢。还可以排除其他可能的弛豫机制(扩散运动、O - H弛豫或与溶解的双氧分子的电子自旋S = 1的耦合)。
有明确证据表明顺势疗法溶液不能像通常假设的那样被视为纯水。相反,我们证明了在物质(水、乳糖、铜、钩吻素)稀释/增效时存在明显的记忆效应,这通过不同的旋转相关时间和平均H⋯H距离反映出来。这种记忆效应的一种可能解释可能在于量子场论所暗示的,由真空电磁场的零点涨落介导的纳米颗粒和/或纳米气泡周围介观水结构的形成。我们的数据不支持顺势疗法制备的药物存在阿伏伽德罗“壁”的观点。相反,似乎所有稀释都具有由增效物质、容器的化学性质、溶解气体和电磁环境决定的特定物质构型。顺势疗法制备的药物对电磁场的这种敏感性可能会因顺势疗法药物制备中常规应用的高度非线性处理而放大。在这些方向上需要进一步的研究。现在是揭开顺势疗法药物制备神秘面纱的时候了。