Mesoporous Silica: for solubility enhancement of challenging compounds
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Silica
Formulation Development and Evaluation of Brivaracetam Extended- Release Tablets by QbD Approach
Press Release
Abstract
This research article outlines a systematic and science-based approach to formulate extended-release tablets of brivaracetam (BRV) by means of quality by design (QbD) method. BRV, a potent antiepileptic drug, faces challenges due to its short half-life, necessitating…
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For the good of the patient: Silica & Silicates from Evonik in the pharmaceutical industry
Many challenges – one solution: Fumed silica as well as precipitated silica and silicates from Evonik are some of the most important and highly utilized pharmaceutical excipients. Whether you manufacture medicines for solid, semi-solid or liquid dosing, we support you at every stage of product…
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Use of Liquid Solid Technique for Development and Evaluation Study of Nifedipine Tablets to Enhance…
Abstract
Objectives: The current research finding suggests dissolution enhancement of nifedipine tablets using Liquid solid technique.
Materials and Methods: The drug's solubility in various liquid carriers has been examined, out of which drug shows maximum solubility in PEG 400 which acts…
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Evaluation of AaltoCell as a filler for tablets compressed from high-shear wet granulated…
Abstract
Microcrystalline cellulose (MCC) is a purified, partially depolymerized cellulose, which is obtained by treating αcellulose with mineral acids. Ever since the first microcrystalline cellulose was commercialized, different grades of microcrystalline cellulose have widely been used in the…
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Design and evaluation of solid self-nanoemulsifying drug delivery systems of cyclosporine developed…
Abstract
Cyclosporine (CYC) is a drug that belongs to the BCS class II category. This study was designed to develop novel solid self-nanoemulsifying drug delivery systems (S-SNEDDS) for cyclosporine (CYC), using chitosan–EDTA microparticles. Such microparticles are known to exhibit superior…
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FT-NIR models for predicting film quality parameters in titanium dioxide-free tablet coatings
Abstract
This study leverages Fourier Transform Near-Infrared (FT-NIR) spectroscopy to monitor the coating process of pharmaceutical tablets using PVA-based TiO2-free films, with talc and iron oxides as opacifiers. By employing a combination of multivariate analytical techniques to evaluate the…
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Advanced Oral Breviscapine Sustained-Release Tablets for Improved Ischemic Stroke Treatment
Abstract
This study aimed to address the challenges associated with the low oral bioavailability and the necessity for frequent dosing of breviscapine (BRE), a mainstream drug in the treatment of cardiovascular and cerebrovascular diseases. The poor solubility and permeability of BRE in the…
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Envisioning New Concepts for 3D Printing and Solubility Enhancement: Tablet Manufacturing of Loaded…
This poster was presented at the AAPS 2024 by APRECIA and Millipore Sigma
Many new drug substances are poorly soluble, making traditional drug development slow and costly.
This study explores improving solubility using mesoporous silica, which stabilizes drugs within nanosized pores.…
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The composition of Drugs going off-patent in the upcoming years
As a follow up on the article 𝐖𝐡𝐢𝐜𝐡 𝐝𝐫𝐮𝐠𝐬 𝐰𝐢𝐥𝐥 𝐥𝐨𝐬𝐞 𝐩𝐚𝐭𝐞𝐧𝐭𝐬 𝐢𝐧 𝐭𝐡𝐞 𝐜𝐨𝐦𝐢𝐧𝐠 𝐲𝐞𝐚𝐫𝐬? by Joanna Sadowska, PhD, EMBA in which includes over 30 products going off-patent from 2025 to 2037 we pulled together the dosage form and composition of these products. Please note that the composition may vary in…
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In silico formulation optimization and particle engineering of pharmaceutical products using a…
Abstract
Pharmaceutical drug dosage forms are critical for ensuring the effective and safe delivery of active pharmaceutical ingredients to patients. However, traditional formulation development often relies on extensive lab and animal experimentation, which can be time-consuming and costly.…
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