Special Issue "Studies of the Dosage Form and Stability of the Drug by Various Techniques"
Deadline for manuscript submissions: 5 November 2023 | Viewed by 25944
Interests: liquid chromatography; spectrophotometry; densitometry; organic compounds analysis; QSAR; QSRR; QSPR; pharmaceutical analysis; purity of pharmaceutical preparations
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Special Issue in Processes: 10th Anniversary of Processes: Women's Special Issue Series
Special Issue in Processes: Processes in 2023
Stability determines the shelf-life of drugs, during which their pharmacological activities do not decline and any degradation products are nontoxic. The medicinal product remains stable if the declared content of the drug substance does not differ by more than 5%, the decomposition products and microbiological contamination are within the acceptable standards, and there are no changes in the appearance and physical properties of the preparation or drug substance release. Ensuring the stability of a medicinal product begins at the stage of drug substance synthesis, then during technological processes (granulation, tableting), packaging (placing in immediate packaging), distribution (wholesalers, pharmacies) and administration to the patient.
This Special Issue, “Studies of the dosage form and stability of the drug by various techniques”, aims to curate novel advances in the development and application of different analytical techniques in drug analyses. Topics include, but are not limited to:
- the dosage form of the drug and its stability;
- physical factors influencing the shelf life of medicinal products;
- chemical factors influencing the shelf life of medicinal products;
- microbiological factors influencing the shelf life of medicinal products;
- stabilization treatments during drug preparation;
- drug stability study;
- drug purity testing;
- the use of new media in the formulation of a dosage form with model substances;
- influence of the composition of the tablet mass on the availability of micro and macro elements;
- determination of the active substance in medicinal products;
- drug quality assessment;
- dosage form technology.
Prof. Dr. Alina Pyka-Pająk
Manuscript Submission Information
Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All papers will be peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.
Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Processes is an international peer-reviewed open access monthly journal published by MDPI.
Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2000 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.
- drug analysis
- drug stability
- dosage form
- analytical methods
The below list represents only planned manuscripts. Some of these manuscripts have not been received by the Editorial Office yet. Papers submitted to MDPI journals are subject to peer-review.
Title: Modeling and control of albumin-mediated release of corticotropin from a semi-solid drug formulation
Authors: Wioletta Siemiradzka； Barbara Dolińska； Florian Ryszka
Affiliation: Medical University of Silesia
Title: Dosage form and drug stability studies using various techniques
Authors: Barbara Dolińska
Affiliation: Medical University of Silesia