Fig 1 - uploaded by Musa Autamashih
Content may be subject to copyright.
Analysis of samples by scanning electron microscopy. (a) Formulation 1 indicates the ingredients for this novel formulation of ACM by direct compression. (b) Formulation 2 indicates the ingredients for the old traditional formulation of the ACM by wet granulation, and (c) indicates a side-by-side comparison of the structural morphologies of MCC with RMAS particles showing morphological similarity.

Analysis of samples by scanning electron microscopy. (a) Formulation 1 indicates the ingredients for this novel formulation of ACM by direct compression. (b) Formulation 2 indicates the ingredients for the old traditional formulation of the ACM by wet granulation, and (c) indicates a side-by-side comparison of the structural morphologies of MCC with RMAS particles showing morphological similarity.

Source publication
Article
Full-text available
The conventional approach in the tablet formulation of acetaminophen (ACM) suggests the use of five or more different excipients in a wet granulation tableting process. The use of many excipients in tablet formulation may negatively create excipient-excipient interactions, excipient-drug interactions, exaggerated product side effects, and high drug...

Similar publications

Article
Full-text available
Natural polymers are abundantly available in plants with their wider pharmaceutical applications and are preferred more than some synthetic polymers because of their biodegradable, biocompatible and non-toxic properties. The study aims to formulate Itopride Hydrochloride loaded Sustained Release (SR) matrix tablet from the mucilage extracted from o...
Article
Full-text available
In the present research work, Febuxostat Immediate Release Tablet was prepared by direct compression method using varying concentrations of Lycoat, Crospovidone& Croscarmellose sodium as disintegrants. The formulations prepared were evaluated for precompression& post-compression parameters. From the drug excipient compatibility studies, we observe...
Article
Full-text available
Sustained Release is also a promising method for reducing medication side effects by preventing the therapeutic concentration of the drug from fluctuating in the body.The basic rationale of a sustained drug delivery system is to optimise a drug's biopharmaceutical, pharmacokinetic, and pharmacodynamic properties in order to maximise utility, minimi...
Article
Full-text available
The biphasic drug delivery system contains two different release phases-an immediate release phase and an extended-release phase. This type of system is primarily used when maximum relief needs to be achieved quickly and it is followed by sustained release phase to avoid repeated administration. Immediate release tablets containing loading dose (3....
Article
Full-text available
With the aim of developing an in vitro model for the bioavailability (BA) prediction of drugs, we focused on the study of levonorgestrel (LVN) released by 1.5 mg generic and brand-name tablets. The developed method consisted in combining a standard dissolution test with an optimized parallel artificial membrane permeability assay (PAMPA) to gain in...