Results 61 to 70 of about 3,108 (188)

Approaches to Assessing the Quality of Fatty Oils and Medicinal Products Formulated as Oily Solutions

open access: yesРегуляторные исследования и экспертиза лекарственных средств
INTRODUCTION. Vegetable fatty oils can comprise over 50% of a medicinal product formulated as an oily solution (in some cases, 100%). The quality of the vegetable fatty oil used and the processes occurring in this oil have a significant impact on the ...
A. A. Ponomarenko, L. I. Panova
doaj   +1 more source

Plant‐Based Biosynthesis of Metal and Metal Oxide Nanoparticles: An Update on Antimicrobial and Anticancer Activity

open access: yesChemBioEng Reviews, Volume 11, Issue 6, December 2024.
When it comes to finding novel ways to battle newly developing pathogenic strains and illnesses, nanoparticles are the first line of defense. Plant‐based nanoparticles are showing more significance over chemically or physically synthesized nanoparticles. Several plant species and their constituent parts have found several applications in medicine. They
Shruti Nandkishor Tanwar   +4 more
wiley   +1 more source

Standardisation of human immunoglobulin preparations: Harmonising Russian State pharmacopoeia with world quality standards

open access: yesБиопрепараты: Профилактика, диагностика, лечение
INTRODUCTION. Human immunoglobulin preparations (HIP) used in medicine effectively treat autoimmune diseases, inflammatory diseases, and immune deficiencies and prevent diseases of various aetiologies.
O. A. Demidova   +2 more
doaj   +1 more source

Nonclinical safety and immunogenicity assessment of a combined DTacP vaccine in animal models

open access: yesJournal of Applied Toxicology, Volume 44, Issue 11, Page 1689-1699, November 2024.
Abstract The (diphtheria, tetanus, and pertussis [acellular, component] [DTacP]) vaccine is a combined vaccine designed to prevent three potentially fatal diseases including pertussis, tetanus, and diphtheria in both children and adults. We utilized advanced technology to develop a novel DTacP vaccine that was previously unavailable in China.
Shihui Li   +12 more
wiley   +1 more source

Pharmacopoeias’ and manufacturers’ requirements for the quality of hard gelatin capsule shells

open access: yesРегуляторные исследования и экспертиза лекарственных средств
INTRODUCTION. The lack of national requirements regulating the quality of empty hard gelatin capsule shells (before filling with medicines) causes difficulties not only for capsule developers and manufacturers but also for experts evaluating regulatory ...
E. L. Kovaleva   +3 more
doaj   +1 more source

CURRENT REQUIREMENTS FOR THE QUALITY OF HERBAL MEDICINAL PRODUCTS

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2018
The article provides the results of a comparative analysis of requirements laid out in the State Pharmacopoeia of the USSR, XI ed. (SPh XI) and the State Pharmacopoeia of the Russian Federation, XIII ed.
E. I. Sakanyan   +3 more
doaj   +1 more source

Mebendazole spectrophotometric determination: theorical and experimental study of the interaction with sodium hydroxide [PDF]

open access: yes, 2016
USP, EP, and Argentinian Pharmacopoeia proposed HPLC-UV for quantitative quality control of mebendazole (MBZ) tablets. In this work, a spectrophotometric method is proposed.
Delfino, Mario Raul   +3 more
core  

Inhalable fucoidan microparticles combining two antitubercular drugs with potential application in pulmonary tuberculosis therapy [PDF]

open access: yes, 2018
The pulmonary delivery of antitubercular drugs is a promising approach to treat lung tuberculosis. This strategy not only allows targeting the infected organ instantly, it can also reduce the systemic adverse effects of the antibiotics. In light of that,
Ana Grenha   +7 more
core   +2 more sources

Multifunctional nanocarriers for lung drug delivery [PDF]

open access: yes, 2020
Nanocarriers have been increasingly proposed for lung drug delivery applications. The strategy of combining the intrinsic and more general advantages of the nanostructures with specificities that improve the therapeutic outcomes of particular clinical ...
Grenha, Ana, Pontes, Jorge Filipe
core   +2 more sources

The importance of World Health Organization international reference standards in the product life cycle of biosimilars

open access: yesAnnals of the New York Academy of Sciences, Volume 1540, Issue 1, Page 225-234, October 2024.
Abstract Technological advances in analytics, as well as scientific and regulatory knowledge and experience gained from biosimilar development/approvals over the last decade, enabled the World Health Organization (WHO) in 2022 to revise its guidelines on the evaluation of biosimilars.
Hye‐Na Kang   +4 more
wiley   +1 more source

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