2014
DOI: 10.1007/978-1-4939-1519-4_11
|View full text |Cite
|
Sign up to set email alerts
|

Microenvironmental pH Control and Mixed Polymer Approaches to Optimise Drug Delivery with Hydrophilic Matrix Tablets

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
7
0

Year Published

2017
2017
2021
2021

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(7 citation statements)
references
References 70 publications
(93 reference statements)
0
7
0
Order By: Relevance
“…The saturation solubility of CV in distilled water and in phosphate buffer (pH 7.4) was found to be 0.00022±0.0015 and 0.0058±0.0013 mg/ml, respectively. In basic pH, the solubility of CV is poor owing to its basic nature [27] . As it remains in the unionized form in distilled water and in pH 7.4 phosphate buffer, it dissolves at a lower rate in these media.…”
Section: Resultsmentioning
confidence: 99%
“…The saturation solubility of CV in distilled water and in phosphate buffer (pH 7.4) was found to be 0.00022±0.0015 and 0.0058±0.0013 mg/ml, respectively. In basic pH, the solubility of CV is poor owing to its basic nature [27] . As it remains in the unionized form in distilled water and in pH 7.4 phosphate buffer, it dissolves at a lower rate in these media.…”
Section: Resultsmentioning
confidence: 99%
“…A higher hydrophobicity can be a preferable choice for elapsed chemical release in pH neutral microenvironment [58]. In addition, higher deposition rate, thicker and denser with more retaining carbon rings are also important to keep films intact during long time immersion in DI water.…”
Section: Chemical Release Testmentioning
confidence: 99%
“…Most of the available active pharmaceutical ingredients (API) are either weak acids, bases or their salts with dissociation constants within or near the range of the physiological pH values in the GIT. This results in their pH-dependent solubility, which affects the drug absorption process (Timmins et al, 2014). Oral dosage forms are exposed to both acidic and neutral conditions while passing along the digestive tract.…”
Section: Introductionmentioning
confidence: 99%
“…In the case of hydrophilic matrix systems, drug release is a complex interplay between matrix erosion and drug diffusion, with both processes depending on the luminal pH conditions at the absorption site. (Timmins et al, 2014;Siepmann and Peppas, 2001). The solubility of ionizing compounds (i.e.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation