RESUMO
Pullulan (PUL) films containing pomegranate seed oil and Eudragit® RS100 nanocapsules loaded with clotrimazole (CTZ-NC-PUL) were developed to treat vulvovaginal candidiasis (VVC). Our findings showed that the nanocapsule average diameter was around 163 ± 4 nm, with polydispersity index values of up to 0.1 ± 0.01 and positively charged zeta potential (+ 43.5 ± 0.7 mV). The pH was in the acid range (5.14 ± 0.12) and encapsulation efficiency was around 99.6%; CTZ nanoencapsulation promoted higher homogeneity values for the film (91%), and the stability studies displayed no changes in the drug content after 120 days for the CTZ-NC-PUL under refrigerated conditions. All formulations were considered non-irritant, and CTZ-NC-PUL promoted a controlled release of the drug (60% in 24 h) compared to CTZ-PUL (100% in 8 h). The permeation results corroborate the drug release, where higher CTZ amounts were found in the mucosa and receptor medium for CTZ-PUL (21.02 and 4.46 µg/cm2). The films were fast dissolving (10 min), and CTZ-NC-PUL presented higher mucoadhesive properties; the antifungal activity against Candida albicans was maintained, and the in vitro efficacy of the film was proved. In conclusion, CTZ-NC-PUL formulation was considered promising and suitable for vaginal application against candida-related infections.
Assuntos
Candidíase Vulvovaginal , Candidíase , Nanocápsulas , Feminino , Humanos , Gravidez , Clotrimazol/farmacologia , Clotrimazol/uso terapêutico , Antifúngicos/farmacologia , Antifúngicos/uso terapêutico , Candidíase Vulvovaginal/tratamento farmacológico , Candidíase Vulvovaginal/microbiologia , Candida albicans , Candidíase/tratamento farmacológico , Parto ObstétricoRESUMO
Polycystic ovary syndrome is the most common endocrine disorder in women. Today, medicinal plants have been considered by women, especially in the reproductive and pregnancy ages. Multiple drug treatments and the length of the treatment period often lead to incomplete treatment by patients. Therefore, due to the side effects of chemical drugs, this study was conducted to assess investigate the effect of pomegranate seed oil on polycystic ovary syndrome. The prevalence of polycystic ovary syndrome is increasing by 15 to 20% and clinically includes oligomenorrhea or amenorrhea, hirsutism, and often infertility. Databases such as Cochran library, Medline, PubMed, SID, and Science Direct were used to access the related articles. To collect the required information, first, the articles that had one of the keywords of medicinal plants, polycystic ovary syndrome, plant, pomegranate extract, and menstrual irregularities in their text were searched in databases. All studies from 1985 to 2021 are included in the study. Conjugated linolenic acid (CLN) is a group of geometric and positional isomers of linolenic acid in which double bonds are conjugated. CLN has been reported to have a very strong cytotoxic effect on tissue tumor cells in the body, preventing cancer, reducing the accumulation of triacylglycerol in the liver, polycystic ovary syndrome, and LDL cholesterol in the blood. So far, seven CLN isomers have been identified, including ponic acid in pomegranate seed oil. Conjugated linoleic acid (CLA) is a group of situational and geometric isomers of linoleic acid in which double bonds are conjugated. The positive effects of the two main CLA isomers (cis-9, trans-11, and trans-10, cis-12) include inhibiting the growth of cancer, reducing the risk of atherosclerosis, and reducing body fat.
Assuntos
Síndrome do Ovário Policístico , Punica granatum , Feminino , Humanos , Ácido alfa-Linolênico , Óleos de Plantas/farmacologia , Síndrome do Ovário Policístico/tratamento farmacológico , Síndrome do Ovário Policístico/epidemiologiaRESUMO
The combination of pomegranate seed oil and ketoprofen in nanoemulsions aiming to improve the antinociceptive effect was evaluated according to the writhing test and Complete Freud's Adjuvant induced paw inflammation in mice. The formulations showed adequate characteristics and improved ketoprofen's photostability against UVC radiation exposure. The dialysis bag technique showed that 100% of the drug was released from the nanoemulsions after 3h and the oil amount had no influence on the releasing. Furthermore, time- and dose-response curves were obtained to determine the antinociceptive effect of the formulations. In the post-test, the nanoemulsion containing ketoprofen significantly reduced abdominal constrictions in time-response curve, showing effect up to 12h while the free ketoprofen showed effect up to 3h. In addition, the blank nanoemulsion presented a reduction of abdominal constriction up to 1h of pre-treatment. Regarding the dose-response curve, the free ketoprofen presents effect at 0.5mg/Kg dose and nanoemulsion at 1.0mg/Kg dose. Time- and dose-response curves were performed to determine the antinociceptive effect in inflammatory pain. After the evaluation of mechanical allodynia testing at the Von Frey Hair, the free ketoprofen showed effect up to 6h while nanoemulsions presented effect up to 10h. Moreover, acute toxicity was performed with ALT and AST activity evaluations and urea levels. After 7 days of treatment, no toxic effects for nanoemulsions were found. In conclusion, ketoprofen-loaded pomegranate seed oil nanoemulsions presented adequate characteristics and a high antinociceptive activity in the animal models tested.
Assuntos
Analgésicos/uso terapêutico , Anti-Inflamatórios não Esteroides/uso terapêutico , Emulsões/química , Lythraceae/química , Nanopartículas/química , Óleos de Plantas/uso terapêutico , Raios Ultravioleta , Abdome/patologia , Ácido Acético , Analgésicos/administração & dosagem , Analgésicos/farmacologia , Animais , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/farmacologia , Constrição Patológica , Liberação Controlada de Fármacos , Estabilidade de Medicamentos , Adjuvante de Freund , Inflamação/complicações , Inflamação/tratamento farmacológico , Injeções , Cetoprofeno/administração & dosagem , Cetoprofeno/farmacologia , Cetoprofeno/uso terapêutico , Masculino , Camundongos , Atividade Motora/efeitos dos fármacos , Dor/complicações , Dor/tratamento farmacológico , Óleos de Plantas/administração & dosagem , Óleos de Plantas/farmacologia , Sementes/química , Testes de Toxicidade AgudaRESUMO
There has been an increase in the use of botanicals as skin photoprotective agents. Pomegranate (Punica granatum L.) is well known for its high concentration of polyphenolic compounds and for its antioxidant and anti-inflammatory properties. The aim of this study was to analyze the photoprotection provided by P. granatum seed oil nanoemulsion entrapping the polyphenol-rich ethyl acetate fraction against UVB-induced DNA damage in the keratinocyte HaCaT cell line. For this purpose, HaCaT cells were pretreated for 1h with nanoemulsions in a serum-free medium and then irradiated with UVB (90-200 mJ/cm(2)) rays. Fluorescence microscopy analysis provided information about the cellular internalization of the nanodroplets. We also determined the in vitro SPF of the nanoemulsions and evaluated their phototoxicity using the 3T3 Neutral Red Uptake Phototoxicity Test. The nanoemulsions were able to protect the cells' DNA against UVB-induced damage in a concentration dependent manner. Nanodroplets were internalized by the cells but a higher proportion was detected along the cell membrane. The SPF obtained (~25) depended on the concentration of the ethyl acetate fraction and pomegranate seed oil in the nanoemulsion. The photoprotective formulations were classified as non-phototoxic. In conclusion, nanoemulsions entrapping the polyphenol-rich ethyl acetate fraction show potential for use as a sunscreen product.
Assuntos
Acetatos/química , Dano ao DNA/efeitos dos fármacos , Emulsões/farmacologia , Lythraceae/metabolismo , Polifenóis/química , Raios Ultravioleta , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos da radiação , Ensaio Cometa , Dano ao DNA/efeitos da radiação , Emulsões/química , Humanos , Imunoensaio , Interleucina-8/análise , Queratinócitos/citologia , Queratinócitos/metabolismo , Lythraceae/química , Microscopia de Fluorescência , Nanotecnologia , Extratos Vegetais/química , Óleos de Plantas/química , Sementes/química , Sementes/metabolismo , Fator de Proteção SolarRESUMO
This study aimed to prepare pomegranate seed oil nanoemulsions containing ketoprofen using pullulan as a polymeric stabilizer, and to evaluate antitumor activity against in vitro glioma cells. Formulations were prepared by the spontaneous emulsification method and different concentrations of pullulan were tested. Nanoemulsions presented adequate droplet size, polydispersity index, zeta potential, pH, ketoprofen content and encapsulation efficiency. Nanoemulsions were able to delay the photodegradation profile of ketoprofen under UVC radiation, regardless of the concentration of pullulan. In vitro release study indicates that nanoemulsions were able to release approximately 95.0% of ketoprofen in 5h. Free ketoprofen and formulations were considered hemocompatible at 1 µg/mL, in a hemolysis study, for intravenous administration. In addition, a formulation containing the highest concentration of pullulan was tested against C6 cell line and demonstrated significant activity, and did not reduce fibroblasts viability. Thus, pullulan can be considered an interesting excipient to prepare nanostructured systems and nanoemulsion formulations can be considered promising alternatives for the treatment of glioma.
Assuntos
Emulsões/química , Glucanos/química , Cetoprofeno/química , Nanopartículas/química , Óleos de Plantas/química , Células 3T3 , Administração Intravenosa , Animais , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/química , Anti-Inflamatórios não Esteroides/farmacocinética , Antineoplásicos/administração & dosagem , Antineoplásicos/química , Antineoplásicos/farmacocinética , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Relação Dose-Resposta a Droga , Estabilidade de Medicamentos , Glioma/metabolismo , Glioma/patologia , Glioma/prevenção & controle , Hemólise/efeitos dos fármacos , Cetoprofeno/administração & dosagem , Cetoprofeno/farmacocinética , Cinética , Lythraceae/química , Camundongos , Microscopia Eletrônica de Varredura , Estrutura Molecular , Nanopartículas/administração & dosagem , Nanopartículas/ultraestrutura , Fotólise/efeitos da radiação , Ratos , Sementes/química , Raios UltravioletaRESUMO
O objetivo geral deste estudo foi avaliar, em ratos, o efeito do óleo da semente de romã (PSO) sobre o perfil lipídico tecidual e sua influência sobre parâmetros bioquímicos em processos oxidativos. Foi realizada a caracterização do PSO, confirmando a presença do ácido punícico (PA; 55%) como ácido graxo majoritário e a alta concentração de fitosteróis (539mg/100g), bem como a presença de vitamina E (175mg/100g). O PSO apresentou-se dentro dos padrões de qualidade e a sua estabilidade oxidativa foi melhor em comparação ao óleo de linhaça. A suplementação de ratos saudáveis com o PSO, por via intragástrica durante 40 dias, não afetou o ganho de peso total e o peso dos tecidos muscular (gastrocnêmio) e adiposos (epididimal e retroperitonial). No entanto o PA foi metabolizado e incorporado na forma de ácido linoléico conjugado, sendo dose-dependete nos tecidos hepático, muscular, cardíaco, renal e adiposos. No cérebro, não foram observados ácidos graxos conjugados, mas as substâncias reativas ao ácido tiobarbitúrico (TBARS) apresentaram-se significativamente reduzidas nos animais suplementados com PSO, em relação ao controle. De modo geral, os resultados mostram que o PSO não provoca alterações no metabolismo lipídico e não participa do processo de inibição da oxidação em animais saudáveis. Em ratos submetidos ao estresse oxidativo hepático pelo tetracloreto de carbono (CCl4), a suplementação com PSO durante 21 dias não foi capaz de prevenir o quadro de estresse oxidativo, indicando que este óleo não tem efeito antioxidante utilizando esse modelo animal; embora a análise histológica tenha mostrado menores áreas lesionadas no parênquima hepático nos grupos tratados. Os resultados obtidos neste trabalho contribui com a literatura fornecendo mais informações a respeito do uso dos ácidos graxos conjugados, bem como do PSO em organismos saudáveis e submetidos à estresse oxidativo
The aim of this study was to evaluate the effect of pomegranate seed oil (PSO) on tissue lipid profile and its influence on biochemical parameters in oxidative processes of Wistar rats. Characterization of PSO was carried out, confirming the presence of the punicic acid (PA, 55%) as the major fatty acid present in the oil and high concentrations of phytosterols (539mg/100g) were also observed, as well as the presence of vitamin E (175mg/100g). The PSO was within quality standards and it presented a higher oxidative stability as compared to flaxseed oil. The supplementation of healthy rats with the PSO via gavage during 40 days did not affect weight gain and total weight of muscle (gastrocnemius) and adipose (epididymal and retroperitoneal) tissues. However, PA was metabolized and incorporated as CLAs in a dose-dependent manner in the liver, muscle, heart, kidney and adipocytes. In the brain, conjugated fatty acids were not detected, but the values of thiobarbituric acid reactive substances were significantly reduced in animals supplemented with PSO as compared to the control group. Overall, the results showed that the PSO caused no changes in the lipid metabolism and did not inhibit tne oxidation in healthy animals. In rats that underwent hepatic oxidative stress by carbon tetrachloride (CCl4), the PSO supplementation for 21 days was not able to prevent the oxidative stress, indicating that this oil has no antioxidant effect using this animal model; although histological analysis has shown less injured areas in the liver parenchyma in the test groups. The results obtained in this study are a good addition to the literature once it provided more information about the use of conjugated fatty acids as well as garnered useful information about the effects of consumption of PSO in oxidative stress-induced rats