Since the teratogenicity of Thalidomide has been proven, herbal products are more commonly used in pregnancy to not only relieve morning sickness but also to fight infections. These products are frequently considered as natural and therefore harmless. However, herbs contain a number of active substances that, when used during pregnancy, can affect the development of the fetus. Often, pregnant women do not consult the usage of herbal medicines with a physician. The access to these products is easy and treatment of certain ailments with the use of herbs is common in many countries. The aim of the present literature review was to discuss available data regarding the efficacy and safety of cranberry, chamomile, Echinacea purpurea, garlic, ginger, Ginkgo biloba, and peppermint, which are used to counteract the most common ailments during pregnancy, i.e., infections and pregnancy-related ailments (e.g., nausea and vomiting, dizziness, and headache). Analysis of available data showed that ginger is one of the most extensively analyzed herbal remedies. The dose of ginger below 1000 mg per day may help to relief hypereremesis gravidarum, and such an amount of ginger did not increase frequency of adverse effects for either woman or developing fetus. Data regarding other herbs are most often heterogeneous and give conflicting results with no clear conclusions. However, all herbal products should be used with a special caution in pregnancy. Further high-quality human studies should be determined to confirm the safe doses of herbal products which could be used by pregnant or breast-feeding women.

Topical drug delivery in skin diseases provides a non-invasive, direct application of treatments to the affected area and avoids systemic toxicity. Quercetin is a natural polyphenol with documented activity to alleviate the symptoms of many skin diseases. The objective of this study was to prepare and assess the physicochemical properties of hydrogels made of sodium alginate (SA) and cellulose derivatives (methyl cellulose (MC) and carboxymethyl cellulose (CMC)), containing different concentrations of quercetin (0.4 and 0.7%). The physicochemical evaluation of the obtained hydrogels included organoleptic evaluation, texture analysis, spreadability, rheological properties, pH, and stability. Among the prepared formulations, MC-based gels had the highest viscosity, adhesiveness, cohesiveness, and stickiness. The results of this study indicate that MC-based hydrogels were superior to CMC- or SA-based gels in their ability to effectively deliver quercetin to the porcine skin ex vivo. The amount of quercetin retained in the skin after application of MC-based preparations containing higher concentrations of quercetin was 2.04-fold higher for CMC-based hydrogels and 2.6-fold higher for SA-based hydrogels.

In recent years, polyphenols have been extensively studied due to their antioxidant, anticancer, and anti-inflammatory properties. It has been shown that anthocyanins, flavonols, and flavan-3-ols play an important role in the prevention of bacterial infections, as well as vascular or skin diseases. Particularly, resveratrol, as a multi-potent agent, may prevent or mitigate the effects of oxidative stress. As the largest organ of the human body, skin is an extremely desirable target for the possible delivery of active substances. The transdermal route of administration of active compounds shows many advantages, including avoidance of gastrointestinal irritation and the first-pass effect. Moreover, it is non-invasive and can be self-administered. However, this delivery is limited, mainly due to the need to overpassing the stratum corneum, the possible decomposition of the substances in contact with the skin surface or in the deeper layers thereof. In addition, using resveratrol for topical and transdermal delivery faces the problems of its low solubility and poor stability. To overcome this, novel systems of delivery are being developed for the effective transport of resveratrol across the skin. Carriers in the micro and nano size were demonstrated to be more efficient for safe and faster topical and transdermal delivery of active substances. The present review aimed to discuss the role of resveratrol in the treatment of skin abnormalities with a special emphasis on technologies enhancing transdermal delivery of resveratrol.

Open Access Agricultural Journals published by Institute of Agricultural Economics and Information

In the present study, we aimed to determine whether the shelf life of effervescent tablets may be assessed during storage using total directional hemispherical reflectance (THR). We also analyzed selected pharmacopeial parameters of the tablets and used X-ray microtomography to assess the internal structure of the tablets. Two types of effervescent tablets of one commercial product containing magnesium and vitamin B6 (expired and unexpired) were analyzed. In addition, randomly selected unexpired and expired tablets were dried in a vacuum oven for 24 h at 50 °C. The expired effervescent tablets disintegrated in a significantly shorter time than the unexpired tablets (68 s vs. 83 s, p = 0.016). The remaining pharmacopeial parameters did not differ between the two types of tablets. We observed that expired effervescent tablets showed lower mean values of THR in five spectral ranges, which indicates that a greater amount of radiation beam was transmitted into their inner structure than for unexpired tablets. The density of the inner structure assessed on the microtomographic scans differed significantly between all the analyzed tablets (p < 0.001). The highest mean density was observed in the case of the unexpired tablets dried in a vacuum oven (1.273 g/cm³), while the lowest density was observed in the case of the expired tablets (1.261 g/cm³). The expired tablets had a larger pore diameter compared to the unexpired tablets (0.095 mm vs. 0.074 mm, respectively; p = 0.007). Additionally, the percentage of porosity was higher in the expired tablets compared to the unexpired tablets (p < 0.001).

Effects of two independent variables - the content of quercetin (0 or 1 or 1.5 or 5 %) and the content of plasma (0 or 2 or 4 or 6 %) - on the organoleptic properties and rheological parameters of model formulations prepared on an amphiphilic base were estimated. The consistency of all ointments was uniform, and the content of quercetin and plasma lay within the predefined range. Tested ointments are non-Newtonian systems. The content of quercetin and plasma was found to have a significant effect on the rheological properties of the ointments. An increase in the content of plasma in ointments was accompanied by a significant increase in their hardness, viscosity and shear stress and a reduction of their spreadability. The best rheological properties were shown by formulation F-3, containing 1.5 % of quercetin and 2 % of plasma.