Results 1 to 10 of about 7,888,866 (398)

Stability of Dihydroartemisinin-Piperaquine Tablet Halves during Prolonged Storage under Tropical Conditions [PDF]

open access: yes, 2017
Dihydroartemisinin-piperaquine (DP) is recommended for the treatment of uncomplicated malaria, used in efforts to contain artemisinin resistance, and increasingly considered for mass drug administration.
Hodel, Eva Maria
core   +1 more source

The development impact of the illegality of drug trade [PDF]

open access: yes
This paper reviews the unintended consequences of the war on drugs, particularly for developing countries, and weighs them against the evidence regarding the efficacy of prohibition to curb drug use and trade.
Keefer, Philip   +2 more
core  

Drug-Excipient Compatibility Studies in Formulation Development: Current Trends and Techniques [PDF]

open access: yes, 2015
The safety, efficacy, quality and stability of a formulation are the cornerstones of any new drug development process. In order to consistently maintain these attributes in a finished dosage form, it is important to have a comprehensive understanding of ...
Dave, Vivek S   +4 more
core   +1 more source

Mechanochemical Oxidative Degradation of Thienopyridine Containing Drugs: Toward a Simple Tool for the Prediction of Drug Stability. [PDF]

open access: yesACS Cent Sci, 2023
Krake EF   +8 more
europepmc   +1 more source

Entecavir: stability and drug-excipient compatibility [PDF]

open access: yesBrazilian Journal of Pharmaceutical Sciences
Entecavir is an inhibitor of hepatitis B virus (HBV) DNA synthesis that has been widely prescribed in the treatment of chronic infections caused by the virus. Production of generic ETV drugs is an ongoing global endeavor, with particular significance for
Ariadne Botto Fiorot   +4 more
doaj   +1 more source

A novel Malonamide Periodic Mesoporous Organosilica (PMO) for controlled Ibuprofen release [PDF]

open access: yes, 2015
Controlled drug release gained a sharply increasing interest over recent years. Multiple materials have been screened as possible drug carriers, ranging from biodegradable polymers to hydroxyapatite[1].
Clerick, Sander   +5 more
core  

Impact of Quantisal® Oral Fluid Collection Device on Drug Stability. [PDF]

open access: yesFront Toxicol, 2021
Riggio M   +4 more
europepmc   +1 more source

Drug–Phospholipid Co-Amorphous Formulations: The Role of Preparation Methods and Phospholipid Selection

open access: yesPharmaceutics
Background/Objectives: This study aims to broaden the knowledge on co-amorphous phospholipid systems (CAPSs) by exploring the formation of CAPSs with a broader range of poorly water-soluble drugs, celecoxib (CCX), furosemide (FUR), nilotinib (NIL), and ...
Keyoomars Khorami   +3 more
doaj   +1 more source

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