Predicted real solubility (– log x$\text{}_{2}$) and the level of hydrophilic-lipophilic balance (HLB$\text{}_{Requ.}$) of phytochemicals contained in extracts isolated from linden inflorescence (Tiliae flos) with solvents of diversified polarity (ε$\text{}_{M}$)
Predicted real solubility (– log x$\text{}_{2}$) and the level of hydrophilic-lipophilic balance (HLB$\text{}_{Requ.}$) of phytochemicals contained in extracts isolated from linden inflorescence (Tiliae flos) with solvents of diversified polarity (ε$\text{}_{M}$)
Introduction: The broad spectrum of pharmacological properties of linden inflorescence extracts results from polarity and the level of hydrophilic-lipophilic balance of solvents (medium) used to separate compatible phytochemical structures with the expected pharmacotherapeutic profile.
Objective: The use of the general Hildebrand-Scatchard-Fedors theory of solubility to calculate the predicted solubility of classes of phytochemicals contained in linden inflorescences (Tiliae flos) and the indication of those structures which, due to their high solubility in the medium, are responsible for the profile of pharmacological activity.
Material and methods: The Hildebrand, Scatchard equation, supported with computational technique proposed by Fedors, allows calculation of the solubility parameters of the extraction medium. Despite application reservations, it is a fundamental tool for estimating the predictable solubility of phytochemicals in real solution.
Results: The structure of phytochemicals isolated from linden inflorescences (Tiliae flos) owing to the use of solvents of significantly diversified polarity (– dielectric constant – ε$\text{}_{M}$) was the basis for calculating the molar evaporation energy – ΣΔE$\text{}_{i}$ (cal/mol) and molar volume – ΣΔV$\text{}_{i}$ (cm$\text{}^{3}$/mol) by Fedors method, which are fundamental quantities necessary to estimate the solubility parameter– δ$\text{}^{1}\text{}^{/}\text{}^{2}$ and required solubility level of hydrophilic-lipophilic balance – HLB$\text{}_{Requ.}$.
Conclusions: Results of the presented research indicate that basing on the parameters characterizing the structure of phytochemicals and the calculated ideal (–logx$\text{}_{2}^{i}$) and predicted real (–logx$\text{}_{2}$) solubility, it is possible – using the general Hildebrand-Scatchard-Fedors theory of solubility – to choose selectively the cascade of extraction media in order to distinguish in the plant material chemical and structural individuals of different polarity.
Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies
Informacja
SZANOWNI CZYTELNICY!
UPRZEJMIE INFORMUJEMY, ŻE BIBLIOTEKA FUNKCJONUJE W NASTĘPUJĄCYCH GODZINACH:
Wypożyczalnia i Czytelnia Główna: poniedziałek – piątek od 9.00 do 19.00