2016
DOI: 10.1016/j.ijbiomac.2015.10.019
|View full text |Cite
|
Sign up to set email alerts
|

In situ niosome forming maltodextrin proniosomes of candesartan cilexetil: In vitro and in vivo evaluations

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

2
26
1

Year Published

2017
2017
2023
2023

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 46 publications
(30 citation statements)
references
References 25 publications
2
26
1
Order By: Relevance
“…Proniosomes are produced by coating a thin layer of non-ionic surfactant on a water-soluble carrier (2,11,19). To make proniosomes, the water-soluble carriers need to be non-toxic, safe, free-flowing and have good water solubility to allow easy hydration.…”
Section: Types Of Specialized Niosomes 211 Proniosomesmentioning
confidence: 99%
See 1 more Smart Citation
“…Proniosomes are produced by coating a thin layer of non-ionic surfactant on a water-soluble carrier (2,11,19). To make proniosomes, the water-soluble carriers need to be non-toxic, safe, free-flowing and have good water solubility to allow easy hydration.…”
Section: Types Of Specialized Niosomes 211 Proniosomesmentioning
confidence: 99%
“…To make proniosomes, the water-soluble carriers need to be non-toxic, safe, free-flowing and have good water solubility to allow easy hydration. Maltodextrin, sorbitol, mannitol, glucose monohydrate, lactose monohydrate, and sucrose stearate have been used to prepare proniosomes (2,19). Proniosomes present in a dry powder form and have several advantages over the conventional niosomes such as better stability, less likely to form aggregates as well as reduced drug leakage (3).…”
Section: Types Of Specialized Niosomes 211 Proniosomesmentioning
confidence: 99%
“…Niosomes based formulation for enhanced oral bioavailability of candesartan cilexetil [15] Table 1. Presentation of liposome-type systems.…”
Section: Main Components Illustrative Applicationmentioning
confidence: 99%
“…Oral administration is a most preferred route with high patient compliance. However, bioavailability is poor progress observed reasons behind were poor solubility of drug candidate followed by less absorption [2]. Less aqueous solubility is the major drawback encountered with the formulation design of new chemical moiety [3].…”
Section: Introductionmentioning
confidence: 99%