Zobrazeno 1 - 10
of 2 861
pro vyhledávání: '"Immediate-release"'
Autor:
Vishal Gupta, Jitendra Gupta
Publikováno v:
Journal of Applied Pharmaceutical Research, Vol 12, Iss 4, Pp 31-43 (2024)
Background: Blood cancer is a significant contributor to mortality rates worldwide, and its prevalence is projected to rise on a global scale. This trend places considerable strain on healthcare systems and necessitates the expedited development of i
Externí odkaz:
https://doaj.org/article/60a727aafd14479b957589a5fd7ed632
Publikováno v:
Journal of Applied Pharmaceutical Research, Vol 12, Iss 4, Pp 66-74 (2024)
Background: Hypertension is a common complication of type II diabetes. The present research work aimed to develop bilayer tablets that would manage type II diabetes patients with hypertension. The prepared bilayer tablet has an immediate-release laye
Externí odkaz:
https://doaj.org/article/9db110a0f9214d00959c695d24950c6c
Publikováno v:
European Pharmaceutical Journal, Vol 71, Iss 1, Pp 32-42 (2024)
The objective of the present investigation is to improve the solubility of valsartan and prepare immediate release tablets.
Externí odkaz:
https://doaj.org/article/dff7919a714b47f59bc035b34b83eb8d
Autor:
Felicijan Tjaša, Bogataj Marija
Publikováno v:
Acta Pharmaceutica, Vol 74, Iss 2, Pp 269-287 (2024)
Oral solid dosage forms are most frequently administered with a glass of water which empties from the stomach relatively fast, but with a certain variability in its emptying kinetics. The purpose of this study was thus to simulate different individua
Externí odkaz:
https://doaj.org/article/87bc425847d047b0890a14565e124276
Autor:
Poowadon Muenraya, Apichart Atipairin, Teerapol Srichana, Narumon Changsan, Neelam Balekar, Somchai Sawatdee
Publikováno v:
Science and Technology Indonesia, Vol 9, Iss 1, Pp 43-58 (2024)
Montelukast tablets are sold under the brand name Singulair and are used to control and prevent asthma symptoms. In this study,10 mg film-coated montelukast tablets were developed as a generic drug in order to evaluate the pharmaceutical equivalent o
Externí odkaz:
https://doaj.org/article/71845d8238a743de9699f1067378df64
Publikováno v:
Pharmaceutics, Vol 16, Iss 10, p 1324 (2024)
Background/Objectives: Physiologically based pharmacokinetic (PBPK) absorption models are instrumental for assessing drug absorption prior to clinical food effect studies, though discrepancies in predictive and actual outcomes are observed. This stud
Externí odkaz:
https://doaj.org/article/f1c39f2a78504efc9b8667862eea6a9a
Autor:
Morenikeji Aina, Fabien Baillon, Romain Sescousse, Noelia M. Sanchez-Ballester, Sylvie Begu, Ian Soulairol, Martial Sauceau
Publikováno v:
Gels, Vol 10, Iss 10, p 665 (2024)
Precision in dosing is crucial for optimizing therapeutic outcomes and preventing overdosing, especially in preterm infants. Traditional manual adjustments to adapt the dose often lead to inaccuracies, contamination risks, and reduced precision. To o
Externí odkaz:
https://doaj.org/article/eafbd6126ad842daa07c2946134fa8aa
Autor:
Eduardo Agostinho Freitas Fernandes, Joy van Oudtshoorn, Andrew Tam, Liliana Carolina Arévalo González, Erwin Guzmán Aurela, Henrike Potthast, Katalina Mettke, Ryosuke Kuribayashi, Kohei Shimojo, Miho Kasuga, Lázaro Morales, Zulema Rodríguez, Ben Jones, Choongyul Ahn, Eunju Yun, So Hee Kim, Clare Rodrigues, Toh Tiong, Christopher Crane, Chantal Walther, Matthias S. Roost, Tzu-Ling Chen, Li-feng Hsu, April C. Braddy, Alfredo García-Arieta, Ivana Abalos, Milly Divinsky, Abdulaziz Alsuwyeh, Bader Alzenaidy, Adel Alharf
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 27 (2024)
Bioequivalence (BE) studies are considered the standard for demonstrating that the performance of a generic drug product in the human body is sufficiently similar to that of its comparator product. The objective of this article is to describe the rec
Externí odkaz:
https://doaj.org/article/79b11805c0464d5e943c1517544011d9
Autor:
Enes Sarıgedik, Gözde Çakırsoy Çakar, Zafer Ercan, Kenan Evren Öztop, Musa Pınar, Hamad Dheir, Necattin Fırat, Mahmud İslam
Publikováno v:
Sakarya Tıp Dergisi, Vol 13, Iss 3, Pp 478-483 (2023)
Background: This study aimed to investigate whether de novo extended-release tacrolimus (ERT) therapy is safe in kidney recipients. Methods: The study was single-center, retrospective, and included a total of 57 patients, including 30 patients in the
Externí odkaz:
https://doaj.org/article/deaca066868d47c0998184d05a5e5815
Publikováno v:
European Journal of General Practice, Vol 29, Iss 1 (2023)
AbstractBackground The immediacy of the onset of opioids may be associated with the risk of dependency and accidental overdose. Nasal and oromucosal fentanyl dosage forms are so called immediate release fentanyl (IRF). These IRFs have been approved t
Externí odkaz:
https://doaj.org/article/ab14f5c4d0794ac292a33d6cca979c6e