Zobrazeno 1 - 10
of 207
pro vyhledávání: '"Humberto Gomes Ferraz"'
Autor:
Rosana Pereira da Silva, Fanny Judhit Vereau Reyes, Josiane Souza Pereira Daniel, Julia Estevam da Silva Pestana, Samara de Almeida Pires, Humberto Gomes Ferraz
Publikováno v:
Powders, Vol 3, Iss 2, Pp 202-216 (2024)
The consumption of fiber in the human diet is a global recommendation to ensure a healthy diet. Quinoa (Chenopodium quinoa Willd.), a gluten-free grain, and chia (Salvia hispanica), a seed, contain a high fiber content, and both have the potential to
Externí odkaz:
https://doaj.org/article/2e69aba5c94343f0a673ae9c207d9ca2
Publikováno v:
Journal of Pharmacy & Pharmacognosy Research, Vol 10, Iss 5, Pp 847-856 (2022)
Context: In the development of a good analytical method, the selection of appropriate conditions for quantifying drugs is essential. The method validation should be determined before conducting the dissolution test. Aims: To develop and validate t
Externí odkaz:
https://doaj.org/article/637858c2845c43719d06d3040cb22138
Publikováno v:
Pharmaceutics, Vol 15, Iss 11, p 2564 (2023)
D-limonene, derived from citrus essential oils, holds significant therapeutic potential but faces challenges due to its high volatility, especially in pharmaceutical formulations. This study investigates microemulsions as a promising delivery system
Externí odkaz:
https://doaj.org/article/a7a4f4bcdeb8457aa6c14ca191aa8f40
Autor:
Rosmery Merma Leon, Michele Georges Issa, Marcelo Dutra Duque, Josiane Souza Pereira Daniel, Humberto Gomes Ferraz
Publikováno v:
Pharmaceutics, Vol 15, Iss 6, p 1735 (2023)
Hydrochlorothiazide (HTZ) and Valsartan (VAL) are poorly soluble drugs in BCS classes IV and II. This study aimed to develop a method to assess the dissolution profile of tablets containing HTZ (12.5 mg) and VAL (160 mg) as a fixed-dose combination,
Externí odkaz:
https://doaj.org/article/36aba3c0879449a1ba7f055bb8e92afc
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 38, Iss 2, Pp 337-44 (2021)
Generic drugs play an important role in healthcare systems as they represent an effective and more affordable alternative for the population. In Peru, a regulation of interchangeability of generic drugs (also called multisource drugs) was stablished
Externí odkaz:
https://doaj.org/article/c11bab4398a14c75b8b95fe1f76d0a09
Autor:
Rosana Pereira da Silva, Giovanna Sayuri Domingues Kawai, Fabio Ramos Dias de Andrade, Vinicius Danilo Nonato Bezzon, Humberto Gomes Ferraz
Publikováno v:
Solids, Vol 2, Iss 2, Pp 192-211 (2021)
Calcium carbonate (CaCO3) from the seaweed Lithothamnium calcareum is a suitable dietary supplement for the prevention of osteoporosis, due to its chemical composition. This study compared CaCO3 from L. calcareum to CaCO3 from oyster shell and inorga
Externí odkaz:
https://doaj.org/article/0b399190ffb24f7a9567e53df1332bee
Publikováno v:
Pharmaceutics, Vol 15, Iss 5, p 1544 (2023)
This study aimed to develop a biopredictive dissolution method for desvenlafaxine ER tablets using design of experiments (DoE) and physiologically based biopharmaceutics modeling (PBBM) to address the challenge of developing generic drug products by
Externí odkaz:
https://doaj.org/article/885c5b212a4e4fc49f51943eb3803d11
Autor:
Brenda De Espíndola, André O'Reilly Beringhs, Diva Sonaglio, Hellen Karine Stulzer, Marcos Antônio Segatto Silva, Humberto Gomes Ferraz, Bianca Ramos Pezzini
Publikováno v:
Saudi Pharmaceutical Journal, Vol 27, Iss 5, Pp 702-712 (2019)
Liquisolid pellets (LPs) prepared by extrusion-spheronization are promising delivery systems to improve the dissolution rate of poorly water-soluble drugs. However, developing LPs for high dose drugs (e.g. antiretroviral ritonavir, RTV) is a major ch
Externí odkaz:
https://doaj.org/article/4601f6c2c6724093874551e22cd89e9d
Autor:
Asif Ahmad Bhat, Ritu Gilhotra, Yogendra Singh, Sanjay Sharma, Terezinha de Jesus Andreoli Pinto, Humberto Gomes Ferraz, Sachin Kumar Singh, Kamal Dua, Gaurav Gupta
Publikováno v:
Nanomedicine. 18:583-587
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3dfc6d6d13011cdaec36f7834d1cd2d
https://doi.org/10.2217/nnm-2023-0032
https://doi.org/10.2217/nnm-2023-0032
Autor:
Michele Georges Issa, Natalia Vieira de Souza, Bruna Wenyi Chuang Jou, Marcelo Dutra Duque, Humberto Gomes Ferraz
Publikováno v:
Pharmaceutics, Vol 14, Iss 5, p 892 (2022)
The development of extended-release dosage forms with adequate drug release is a challenge for pharmaceutical companies, mainly when the drug presents high solubility, as in Biopharmaceutics Classification System (BCS) class I. This study aimed to de
Externí odkaz:
https://doaj.org/article/45f897d9aac24cf0910014c15f3e6849