Fixed-Dose Combinations for HIV/AIDS, Tuberculosis, and Malaria - Report of a Meeting Held 16-18 December 2003 Geneva
(2003; 199 pages) Ver el documento en el formato PDF
Índice de contenido
Abrir esta carpeta y ver su contenidoSummary: Observations and some ways forward
Abrir esta carpeta y ver su contenidoWelcome
Abrir esta carpeta y ver su contenidoFixed-dose combinations for tuberculosis: lessons learned from a clinical, formulation and regulatory perspective
Abrir esta carpeta y ver su contenidoProduct costs of fixed-dose combination tablets in comparison with separate dispensing and or co-blistering of antituberculosis drugs
Abrir esta carpeta y ver su contenidoFixed-dose combinations: artemisinin-based combination therapies for malaria treatment
Abrir esta carpeta y ver su contenidoDeveloping combinations of drugs for malaria examination of critical issues and lessons learnt
Abrir esta carpeta y ver su contenidoSafety and long-term effectiveness of generic fixed-dose formulations of nevirapine-based HAART amongst antiretroviral-naïve HIV-infected patients in India
Abrir esta carpeta y ver su contenidoEffect of introduction of fixed-dose combinations on the drug supply chain: experiences from the field
Abrir esta carpeta y ver su contenidoEffect of fixed-dose combination (FDC) medications on adherence and treatment outcomes
Abrir esta carpeta y ver su contenidoEffect of fixed-dose combination (FDC) drugs on development of clinical antimicrobial resistance: a review paper
Abrir esta carpeta y ver su contenidoFixed-dose combination (FDC) drugs availability and use as a global public health necessity: intellectual property and other legal issues
Cerrar esta carpetaPharmaceutical development and quality assurance of FDCs
Ver el documentoAbstract
Ver el documentoIntroduction
Ver el documentoPreformulation studies
Ver el documentoSome examples of the relevance of the properties of the API to product formulation!
Ver el documentoGood Manufacturing Practice (GMP)
Ver el documentoIssues that may arise in the formulation of FDCs that do not arise for single entity products include:
Ver el documentoChanges to registered products (variations)
Ver el documentoQuality control of FDCs
Ver el documentoRecommendations
Ver el documentoReferences
Ver el documentoAnnotated agenda
Ver el documentoList of participants
 

Issues that may arise in the formulation of FDCs that do not arise for single entity products include:

- Possible chemical incompatibility between the drugs At -first manufacture On -aging
- Assay of multiple but similar components in a manner that is accurate, precise and specific


In the case of blister products that contain multiple products, control of manufacturing procedures must ensure that packs contain exactly what is intended and that there are no mix-ups. There is precedent for this type of product in sequential oral contraceptives for which a single blister can contain up to four different types of tablet. Multiple containers in a single carton exist for triple combination therapy of gastric ulcers.

Chemical compatibility of drugs with excipients and with each other

Some interactions are predictable given a good knowledge of organic chemistry, whilst others are not as obvious. If the nature of any interaction is known, conditions of manufacture can be adjusted to as to minimise its occurrence.

Some known interactions in the group of drugs of interest at this meeting include:

- Acid/base interactions. Sulphonamides are mildly acidic and can form salts with bases. An interaction between sulfamethoxazole and trimethoprim is known and has caused manufacturing problems for combinations of these drugs. Stability problems could also result in the form of altered dissolution rate on aging if a reaction occurs slowly. Other such interactions could occur under certain conditions, for example between sulfadoxine and pyrimethamine.

- Schiff's base formation occurs between primary amines and carbonyl-containing molecules. Flavouring agents commonly contain aldehydes and ketones that can potentially react with primary amines such as lamivudine, primoquine, trimethoprim and pyrimethamine.

- When the primary amine component of a hydrazine reacts with a carbonyl group, the resulting compound is called a hydrazone. This reaction is the basis of the reduced bioavailability of isoniazid in the presence of food.


Consequently carbonyl-containing excipients (such as reducing sugars and many flavouring agents) are best avoided in the formulation of drugs that contain primary amine and hydrazine moieties, including isoniazid, lamivudine, primoquine, trimethoprim and pyrimethamine.

- The Maillard reaction and Amadori rearrangement have been proposed in relation to pharmaceuticals, including fluoxetine34 but, at least in that case, was not in practice a problem.

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Última actualización: le 3 mayo 2013