Compatibility studies of Olanzapine pre-formulated with excipients by thermal analysis: preliminary study

Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to investigate drug-excipient interactions and, in consequence, their compatibility. For this purpose, binary mixtures of olanzapine drug substance and the excipients croscarmellose sodium, magnesium stearate and microcrystalline cellulose, were prepared and analysed. By the analysis of the binary mixtures DSC and TG curves it were observed changes on the temperature and enthalpy values of the drug melting and decomposition peak, with the likely formation of intermediate substances.Colegio de Farmacéuticos de la Provincia de Buenos Aire

Effectiveness of different cellulose-based filtration materials against inhalation of SARS-CoV-2-like particles

The respiratory protection equipment (RPE) used by health professionals consists of an essential device to prevent infectious diseases, especially those caused by biological agents such as the coronavirus (SARS-CoV-2). The current epidemiological panorama is worrying, and the context of creation and production of the mask has emerged as an alternative to RPE to face the public health crisis worldwide. The aim of this work is to present a low-cost alternative as an FFP2-like filter for a reusable respirator face mask. This study presents the comparison of different cellulose-based filtering materials performed by retention testing, time saturation testing, aerosol penetration testing, nanoparticle (~140 nm) filtration testing, bacterial filtration efficiency (BFE), analysis of material morphology and usability. The reusable respirator face mask used in this study is an open-source innovation, using 3D printing. Cotton disc proved to be the best filter material for the reusable mask, with satisfactory results and a performance similar to that shown by the N95-type mask. The cotton disc ensured effectiveness over 6 h of use, and after that, the reusable respirator face mask (here, Delfi-TRON®) needed to be sanitized and replenished with a new cotton disc. Upon preliminary analyses of filtration efficiency, the selected filter was shown to be a low-cost biodegradable and biocompatible alternative.info:eu-repo/semantics/publishedVersio

Effect of a gel containing pilocarpine on vaginal atrophy in castrated rats

OBJECTIVES: To evaluate the effect of Carbopol gel formulations containing pilocarpine on the morphology and morphometry of the vaginal epithelium of castrated rats. METHODS: Thirty-one female Wistar-Hannover rats were randomly divided into four groups: the control Groups I (n=7, rats in persistent estrus; positive controls) and II (n=7, castrated rats, negative controls) and the experimental Groups, III (n=8) and IV (n=9). Persistent estrus (Group I) was achieved with a subcutaneous injection of testosterone propionate on the second postnatal day. At 90 days postnatal, rats in Groups II, III and IV were castrated and treated vaginally for 14 days with Carbopol gel (vehicle alone) or Carbopol gel containing 5% and 15% pilocarpine, respectively. Next, all of the animals were euthanized and their vaginas were removed for histological evaluation. A non-parametric test with a weighted linear regression model was used for data analysis (

Compatibility studies of Olanzapine pre-formulated with excipients by thermal analysis: preliminary study

Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to investigate drug-excipient interactions and, in consequence, their compatibility. For this purpose, binary mixtures of olanzapine drug substance and the excipients croscarmellose sodium, magnesium stearate and microcrystalline cellulose, were prepared and analysed. By the analysis of the binary mixtures DSC and TG curves it were observed changes on the temperature and enthalpy values of the drug melting and decomposition peak, with the likely formation of intermediate substances.Colegio de Farmacéuticos de la Provincia de Buenos Aire

Formulation technology of a probiotic (Zymomonas mobilis) in gelatinous capsules

Este estudio tuvo como objetivo la obtención de un probiótico en la forma farmacéutica cápsula utilizando como materia prima Zimomonas mobilis fermentado. La liofilización del fermentado de Z. mobilis en una solución crioprotectora (10% de sacarosa, 1% de gelatina y 4% de dióxido de silicio coloidal) resultó ser la mejor formulación alcanzada. Las cápsulas obtenidas a partir de este producto liofilizado presentaron uniformidad de masa, tiempo de disgregación y disolución satisfactorios, además de un bajo porcentaje de humedad en el lote a escala de laboratorio, al igual que para el lote a escala semi-industrial. El proceso tecnológico utilizado no alteró la viabilidad de las células de Z. mobilis.This study aimed the obtainment of a probiotic in the pharmaceutical form of capsules by using fermented Zymomonas mobilis standardized as raw matter. Lyophilization of the fermented Z. mobilis with a cryoprotective solution (10% saccharose, 1% gelatin and 4% colloidal silicon dioxide) resulted on the best formulation obtained. The capsules obtained from that product of lyophilization had uniform weight, satisfactory time of desintegration and dissolution, and low humidity content, both in the laboratory scale and in the transposition to the semi-industrial scale. The technological processes used did not alter Z. mobilis cell viability.Colegio de Farmacéuticos de la Provincia de Buenos Aire

Effect of a gel containing pilocarpine on vaginal atrophy in castrated rats

OBJECTIVES: To evaluate the effect of Carbopol gel formulations containing pilocarpine on the morphology and morphometry of the vaginal epithelium of castrated rats. METHODS: Thirty-one female Wistar-Hannover rats were randomly divided into four groups: the control Groups I (n=7, rats in persistent estrus; positive controls) and II (n=7, castrated rats, negative controls) and the experimental Groups, III (n=8) and IV (n=9). Persistent estrus (Group I) was achieved with a subcutaneous injection of testosterone propionate on the second postnatal day. At 90 days postnatal, rats in Groups II, III and IV were castrated and treated vaginally for 14 days with Carbopol gel (vehicle alone) or Carbopol gel containing 5% and 15% pilocarpine, respectively. Next, all of the animals were euthanized and their vaginas were removed for histological evaluation. A non-parametric test with a weighted linear regression model was used for data analysis (p<0.05). RESULTS: The morphological evaluation showed maturation of the vaginal epithelium with keratinization in Group I, whereas signs of vaginal atrophy were present in the rats of the other groups. Morphometric examinations showed mean thickness values of the vaginal epithelium of 195.10±12.23 μm, 30.90±1.14 μm, 28.16±2.98 μm and 29.84±2.30 μm in Groups I, II, III and IV, respectively, with statistically significant differences between Group I and the other three groups (p<0.0001) and no differences between Groups II, III and IV (p=0.0809). CONCLUSION: Topical gel formulations containing pilocarpine had no effect on atrophy of the vaginal epithelium in the castrated female rats

Nanoparticles Obtained from Zein for Encapsulation of Mesalazine

We encapsulated MSZ in zein nanoparticles (NP-ZN) using a desolvation method followed by drying in a mini spray dryer. These nanoparticles exhibited a size of 266.6 &plusmn; 52 nm, IPD of 0.14 &plusmn; 1.1 and zeta potential of &minus;36.4 &plusmn; 1.5 mV, suggesting colloidal stability. Quantification using HPLC showed a drug-loaded of 43.8 &micro;g/mg. SEM demonstrated a spherical morphology with a size variation from 220 to 400 nm. A FTIR analysis did not show drug spectra in the NPs in relation to the physical mixture, which suggests drug encapsulation without changing its chemical structure. A TGA analysis showed thermal stability up to 300 &deg;C. In vitro release studies demonstrated gastroresistance and a sustained drug release at pH 7.4 (97.67 &plusmn; 0.32%) in 120 h. The kinetic model used for the release of MSZ from the NP-ZN in a pH 1.2 medium was the Fickian diffusion, in a pH 6.8 medium it was the Peppas&ndash;Sahlin model with the polymeric relaxation mechanism and in a pH 7.4 medium it was the Korsmeyer&ndash;Peppas model with the Fickian release mechanism, or &ldquo;Case I&rdquo;. An in vitro cytotoxicity study in the CT26.WT cell line showed no basal cytotoxicity up to 500 &mu;g/mL. The NP-ZN showed to be a promising vector for the sustained release of MSZ in the colon by oral route