Although proteins are often frozen during processing or freeze-dried after formulation to improve their stability, they can undergo degradation leading to losses in biological activity during the process. During freezing, the physical environment of a protein changes dramatically leading to the development of stresses that impact protein stability. Low temperature, freeze-concentration, and ice formation are…
Pharmaceutical Development and Technology Template
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About the Pharmaceutical Development and Technology format
Pharmaceutical Development and Technology is a peer-reviewed journal published by Taylor & Francis, covering Drug Solubulity and Delivery Systems, Advanced Drug Delivery Systems, Advancements in Transdermal Drug Delivery.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Pharmaceutical Development and Technology 12 (3): 45–58.
Formats any DOI in Pharmaceutical Development and Technology style. No sign-up. |
| Publishes research in | Drug Solubulity and Delivery Systems Advanced Drug Delivery Systems Advancements in Transdermal Drug Delivery Analytical Methods in Pharmaceuticals Protein purification and stability |
| ISSN | 1083-7450 |
| Citation impact (2-yr) | 2.73 |
| h-index | 84 |
| i10-index | 1,605 |
| Total citations | 56,957 |
| Top institutions publishing here | Cairo University |
| Journal website | www.informapharmascience.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Pharmaceutical Development and Technology per year
Citation impact of Pharmaceutical Development and Technology by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Pharmaceutical Development and Technology
Drug powders containing micron-size drug particles are used in several pharmaceutical dosage forms. Many drugs, especially newly developed substances, are poorly water soluble, which limits their oral bioavailability. The dissolution rate can be enhanced by using micronized drugs. Small drug particles are also required in administration forms, which require the drug in micron-size size due…
This paper proposes the development of a drug product Manufacturing Classification System (MCS) based on processing route. It summarizes conclusions from a dedicated APS conference and subsequent discussion within APS focus groups and the MCS working party. The MCS is intended as a tool for pharmaceutical scientists to rank the feasibility of different processing routes…
The purpose of this research was to investigate the shape and morphology of various spray-dried protein powders as a function of spray-drying conditions and protein formulations. A benchtop spray dryer was used to spray dry three model proteins in formulation with a sugar or a surfactant. Physical characterizations of the powder included morphology (scanning electron…
A guide for stabilization of pharmaceuticals to oxidation is presented. Literature is presented with an attempt to be a ready source for data and recommendations for formulators. Liquid and solid dosage forms are discussed with options including formulation changes, additives, and packaging documented. In particular, selection of and methods for use of antioxidants are discussed…