2021
DOI: 10.3390/polym13234078
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Highly Efficient Synthesis of Type B Gelatin and Low Molecular Weight Chitosan Nanoparticles: Potential Applications as Bioactive Molecule Carriers and Cell-Penetrating Agents

Abstract: Gelatin and chitosan nanoparticles have been widely used in pharmaceutical, biomedical, and nanofood applications due to their high biocompatibility and biodegradability. This study proposed a highly efficient synthesis method for type B gelatin and low-molecular-weight (LMW) chitosan nanoparticles. Gelatin nanoparticles (GNPs) were synthesized by the double desolvation method and the chitosan nanoparticles (CNPs) by the ionic gelation method. The sizes of the obtained CNPs and GNPs (373 ± 71 nm and 244 ± 67 n… Show more

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Cited by 10 publications
(8 citation statements)
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“…Due to the insolubilisation of chitosan, precipitation occurs. To harden the nanoparticles with an average range of 373 ± 71 nm, glutaraldehyde is applied last [ 52 , 93 , 94 ]. This technique has several advantages over other methods, the most notable of which is its ability to create nanoparticles in a single step, in addition to its low costs, low use of electricity, and frequency [ 95 , 96 ].…”
Section: Production Of Chitosan Nanoparticlesmentioning
confidence: 99%
“…Due to the insolubilisation of chitosan, precipitation occurs. To harden the nanoparticles with an average range of 373 ± 71 nm, glutaraldehyde is applied last [ 52 , 93 , 94 ]. This technique has several advantages over other methods, the most notable of which is its ability to create nanoparticles in a single step, in addition to its low costs, low use of electricity, and frequency [ 95 , 96 ].…”
Section: Production Of Chitosan Nanoparticlesmentioning
confidence: 99%
“…One of the most employed natural polymers for therapeutic hydrogels is chitosan, a biomaterial that can be obtained from the partial deacetylation of naturally abundant chitin [ 34 , 35 , 36 , 37 ]. Along with a strong inherent adhesiveness and biocompatibility, chitosan exhibits desirable hemostatic, antimicrobial, and analgesic properties, making it an attractive material for numerous applications in nanomedicine [ 38 , 39 ] and regenerative medicine [ 40 ]. Moreover, chitosan can be further engineered for specific functionalities by conjugating functional molecules to the free acetamide and hydroxyl groups linked to the glucopyranose rings in their structure, which are susceptible to nucleophilic attacks [ 37 ].…”
Section: Introductionmentioning
confidence: 99%
“…CNPs were synthesized following the ionic gelation method [ 63 ]. Briefly, 2.4 mg/mL of LMW Chitosan (50–190 kDa, deacetylation degree of 75–85%, CAS 9012-76-4) was dissolved in acetic acid 2% v / v under magnetic stirring for 3 h. This procedure protonates the amine groups of monomers and therefore increases its solubility.…”
Section: Materials and Methodsmentioning
confidence: 99%