A polymeric carrier has high potential as active ingredient delivery vehicle owing to its biocompatibility and biodegradability. In this work, pH dependency of the oppositely charged polymers in forming nanoparticle was investigated. A positively charged chitosan and a negatively charged κ-carrageenan were mixed at varied mass ratios (v/v) with a pH ranged from 3 to 6, respectively, to form nanoparticles through polyelectrolyte complexation. The main interest of this research, is to evaluate the effect of pH on the formation of stable active ingredients encapsulated nanoparticle for sustained release. Based on the FTIR result, the presence of new absorption band at 1584 cm−1 and slight shift in the spectrum, indicated the complexation of th...
The nanoparticle drug delivery systems are a promising strategy to avoid the adverse conventional ef...
Nanoparticles (NPs) have an outstanding position in pharmaceutical, biological, and medical discipli...
The oral route administration of protein and peptide drug has been limited by low bioavailability du...
The present study aims to develop a pH thermosensitive nanocarriers as a drug delivery system to bet...
The use of polymeric nanoparticles, especially those composed of natural polymers, has become a very...
Oral drug delivery is widely used in the treatment of oral disease. Due to the complexity of the gas...
The mutually conflicting surface charge requirements for nanoparticles to have long circulation and ...
[[abstract]]In this research, thermo- and pH-responsive nanoparticles with an average diameter of ab...
Mesoporous silica nanoparticles (MSN) offer so many advantages as drug carrier, including large surf...
Chitosan is extensively used in medicine and medical textiles for drug delivery and other applicatio...
ABSTRACT: Nanoparticles of ~10 nm in diameter made with chitosan or lactic acid-graftedchitosan were...
In the past, tripolyphosphate (TPP)-crosslinked chitosan (CS) nanoparticles (CSNPs) have been widely...
Copyright © 2013 Haliza Katas et al. This is an open access article distributed under the Creative C...
[[abstract]]Environmentally sensitive polysaccharide nanoparticles (NPs) were prepared by in situ po...
Chitosan and chitosan derivative-based nanoparticles loaded with insulin were prepared by self-assem...
The nanoparticle drug delivery systems are a promising strategy to avoid the adverse conventional ef...
Nanoparticles (NPs) have an outstanding position in pharmaceutical, biological, and medical discipli...
The oral route administration of protein and peptide drug has been limited by low bioavailability du...
The present study aims to develop a pH thermosensitive nanocarriers as a drug delivery system to bet...
The use of polymeric nanoparticles, especially those composed of natural polymers, has become a very...
Oral drug delivery is widely used in the treatment of oral disease. Due to the complexity of the gas...
The mutually conflicting surface charge requirements for nanoparticles to have long circulation and ...
[[abstract]]In this research, thermo- and pH-responsive nanoparticles with an average diameter of ab...
Mesoporous silica nanoparticles (MSN) offer so many advantages as drug carrier, including large surf...
Chitosan is extensively used in medicine and medical textiles for drug delivery and other applicatio...
ABSTRACT: Nanoparticles of ~10 nm in diameter made with chitosan or lactic acid-graftedchitosan were...
In the past, tripolyphosphate (TPP)-crosslinked chitosan (CS) nanoparticles (CSNPs) have been widely...
Copyright © 2013 Haliza Katas et al. This is an open access article distributed under the Creative C...
[[abstract]]Environmentally sensitive polysaccharide nanoparticles (NPs) were prepared by in situ po...
Chitosan and chitosan derivative-based nanoparticles loaded with insulin were prepared by self-assem...
The nanoparticle drug delivery systems are a promising strategy to avoid the adverse conventional ef...
Nanoparticles (NPs) have an outstanding position in pharmaceutical, biological, and medical discipli...
The oral route administration of protein and peptide drug has been limited by low bioavailability du...