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Block copolymer micelles as ocular drug delivery systems
Abstract
Block copolymer micelles, formed by the self-assembly of amphiphilic polymers, address formulation challenges, such as poor drug solubility and permeability. These micelles offer advantages including a smaller size, easier preparation, sterilization, and superior solubilization, compared…
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QbD-based formulation development of resveratrol nanocrystal incorporated into soluble mesoporous…
Resveratrol (RSV) has powerful antioxidant activities. However, the bioavailability is still limited due to low solubility and transport issues. Nanocrystal technology has been introduced to address these issues; however, the bulky formulation of the nanocrystal process through nanosuspension faces…
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Solid self-nanoemulsifying drug delivery systems of nimodipine: development and evaluation
Abstract
Background
This study aimed to formulate solid self-nanoemulsifying drug delivery systems (SNEDDS) for nimodipine (NIM). The selection of Cremophor RH 40, Lipoxol 300, and PEG 400 as oil, surfactant, and co-surfactant was based on solubility and self-emulsification assessments. A ternary…
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Formulation, optimization, and evaluation of non-propellent foam-based formulation for burn wounds…
Abstract
Burn injuries worldwide pose significant health risks due to frequent microbial infections, which worsen complications and increase mortality rates. The conventional antimicrobial formulations are available in the form of ointments and creams. These formulations are very greasy and stick…
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VIVACOAT® free – Experience the future of Titanium Dioxide coating replacement!
Experience the future of Titanium Dioxide (TiO2) replacement!
Discover bright white films and brilliant colors at reasonable weight gains even on your darkest tablet cores!
Enjoy the freedom of choice when banning TiO2 from your tablet coatings:
TiO2 -free Low…
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Physico-Mechanical and Tableting Properties of Metronidazole Obtained by Crystallo Co-Agglomeration…
Abstract
Background: Due to its simplicity and cost-effectiveness, direct compression has become the approach most frequently used to create tablet. Nonetheless, the active pharmaceutical ingredient should have acceptable flow and good compaction qualities in order to use direct compression in…
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Development of monoclonal antibodies in tablet form: A new approach for local delivery
Abstract
Among the various pharmaceutical forms, tablets offer numerous advantages, like ease of administration, cost-effectiveness in production, and better stability of biomolecules. Beyond these benefits, the tablet form opens up possibilities for alternative routes for the local delivery of…
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Importance of β-cyclodextrin substitution level and type for solubilization and stabilization of…
This poster was presented at CRS 2024 in Bologna
Introduction
Parenteral formulations often contain higher concentrations of excipients than active ingredients. These excipients enhance safety, provide solubility, better stability, increase bioavailability, improve patient compliance, or generally…
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Inclusion complex of 2-phenylethanol in β-cyclodextrin: preparation, characterization, computational…
In the present research, we employed advanced technologies, developing new investigations aiming to obtain simple and inexpensive molecules to reduce pain sensation. For the first time, the inclusion complex of 2-phenylethanol (2-PE) and β-cyclodextrin (β-CD) was achieved (using a spray drying) and…
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Design, Optimization, and Characterization of Zolmitriptan Loaded Liposomal Gels for Intranasal…
Zolmitriptan is the primary drug for the treatment of Migraine. However, the bioavailability of the drug is low and requires repetitive administration leading to side effects. Zolmitriptan's bioavailability can be improved by incorporating it into liposomes as a topical intranasal gel. The…
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