Pharma Excipients
Polyethylene Glycol
3D Printing of Tailored Veterinary Dual-Release Tablets: A Semi- Solid Extrusion Approach for…
Abstract
Metoclopramide (MCP) is frequently used to control nausea and vomiting in animals, but its short half-life requires it to be administered thrice daily. In addition, commercial veterinary MCP formulations are currently lacking. As a result,
veterinary practitioners often resort to…
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Investigation of bioavailability and anti-pancreatic cancer efficacy of a self-nanoemulsifying…
Abstract
Aims
A new self-nanoemulsifying drug delivery system (SNEDDS) was developed for erlotinib (Ert) oral delivery.
Highlights
A pseudo-ternary phase diagram for olive oil, Tween 80 and PEG 600 was constructed.
A SNEDDS composed of 10% olive oil, 20% Tween 80 and 70% (V)…
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Enhancing the Photothermal Properties of Indocyanine Green in Melanoma Spheroids via Encapsulation…
Abstract
Indocyanine green (ICG), a well-known photosensitiser, has shown potential in photothermal therapy (PTT) for cancer treatment, but its effectiveness is limited by poor skin penetration and rapid clearance. To address this, lipid nanocapsules (LNCs) were used as nanocarriers to enhance…
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HME coupled with FDM 3D printing of a customized oral solid form to treat pediatric epilepsy
Abstract
Interest in hot-melt extrusion (HME) and fused deposition material (FDM) printing has increased in recent years, for the production of tailored medications for patients with specific requirements, such as pediatrics. Liquid forms are often preferred for children but these forms are less…
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Development of tablet formulations containing genistein solid dispersion optimized using Box-Behnken…
Abstract
Genistein, a bioactive isoflavone, offers therapeutic potential but is hindered by poor water solubility, limiting its oral bioavailability. This study aimed to enhance genistein’s solubility by developing solid dispersion (SD) and formulating them into tablets. The SDs were prepared using…
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Recent progress in pharmaceutical excipients as P-glycoprotein inhibitors for potential improvement…
Abstract
Pharmaceutical excipients such as P-glycoprotein inhibitors can also increase the solubility and affinity of drugs to the intestinal membrane, enhance paracellular pathways and endocyte uptake, and activate lymph transport pathways, thereby increasing the bioavailability of oral drugs.…
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Effect of formulation composition on trastuzumab stability
Abstract
For monoclonal antibody drug products as for other biologics, while the innovator drug products first becomes commercially available, they are often followed by one or more biosimilar products. These biosimilars often differ from the innovator product, as well as from each other, in…
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Innovative bioinks for 3D bioprinting: Exploring technological potential and regulatory challenges
Abstract
The field of three dimensional (3D) bioprinting has witnessed significant advancements, with bioinks playing a crucial
role in enabling the fabrication of complex tissue constructs. This review explores the innovative bioinks that are
currently shaping the future of 3D bioprinting,…
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Solid Self-Microemulsifying Drug Delivery System for Improved Oral Bioavailability of Relugolix:…
Abstract
Purpose: To improve the oral absorption of relugolix (RLGL), which has low oral bioavailability due to its low solubility and being a substrate of P-glycoprotein (P-gp). A solid self-microemulsifying drug delivery system of relugolix (RLGL-S-SMEDDS) was prepared and evaluated in vitro and…
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Bedaquiline loaded Soluplus® Micelles for Improving Solubility and Intestinal Permeability:…
Abstract
Oral delivery of bedaquiline is the preferred route of drug delivery in the treatment of multidrug-resistant tuberculosis, although its poor bioavailability leads to poor patient compliance. To overcome this problem, we have prepared bedaquiline loaded Soluplus® micelles to improve the…
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