Relevant bibliographies by topics / Ionotropic emulsion-gelation method

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Academic literature on the topic 'Ionotropic emulsion-gelation method'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Ionotropic emulsion-gelation method"

1

Nguyen, G. H., and X. T. Le. "Palmarosa essential oil encapsulated in chitosan nanoparticles by ionotropic gelation: formulation and characterization." IOP Conference Series: Earth and Environmental Science 947, no. 1 (2021): 012002. http://dx.doi.org/10.1088/1755-1315/947/1/012002.

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Abstract In this study, chitosan nanoparticles containing palmarosa essential oil (PEO-CNPs) were formed by ionotropic gelation, consisting of two parts: emulsion preparation followed by ionotropic gelation encapsulation with tripolyphosphate ions (TPP) as a crosslinker. The encapsulation method was optimized by varying three parameters, including chitosan concentration, initial oil loading in the emulsion and TPP concentration. The effects of these parameters on the encapsulation efficiency (EE) and loading capacity (LC) were analyzed. EE had an initial increase followed by a decrease in the
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2

Ritthidej, Garnpimol C., W. Pichayakorn, Chulalongkorn Kusonwiriyawong, and V. Lipipun. "Preparation of Chitosan Nanoparticles for Protein Delivery by w/o/w Emulsion Solvent Evaporation and Simple Ionotropic Gelation Techniques." Solid State Phenomena 121-123 (March 2007): 751–54. http://dx.doi.org/10.4028/www.scientific.net/ssp.121-123.751.

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The purpose of this study was to prepare chitosan nanoparticles (CS NP) for controlled protein delivery. Two techniques, simple ionotropic gelation (method [I]) and w/o/w emulsion solvent evaporation containing ionotropic gelation (method [II]), were used to prepare CS NP. Tripolyphosphate (TPP) and Eudragit L100-55 (Eud) were used as anionic agents to form complex with cationic chitosan. Bovine serum albumin (BSA) was encapsulated into NP. The morphological characteristics, particle size and size distribution, protein entrapment efficiency, zeta potential, in vitro release, protein secondary
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3

S, Revathi, and Dhanaraju Md. "FABRICATION AND EFFECT OF PROCESS VARIABLES OF SITAGLIPTIN MICROSPHERES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 4 (2018): 291. http://dx.doi.org/10.22159/ajpcr.2018.v11i4.24068.

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Objective: The study is to formulate and assess the effects of different variables on the release profile of sitagliptin microspheres.Methods: The microspheres were prepared by emulsion-solvent diffusion method and ionotropic gelation method using ethyl cellulose and sodium alginate as the polymers, respectively. The formulations are optimized by applying 23 factorial design based on the drug-polymer ratio, stirring speed, and method of preparation.Results: The drug-polymer interaction was checked by the Fourier-transform infrared spectroscopy and differential scanning calorimetry the results
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4

Lee, Boon-Beng, Bhesh R. Bhandari, Su Hung Ching, and Tony Howes. "Improving Hydrophilic Barriers of Encapsulated Compounds in Ca-Alginate Microgel Particles through a New Ionotropic Gelation Method for Double Emulsion Droplets." Food Biophysics 14, no. 4 (2019): 365–82. http://dx.doi.org/10.1007/s11483-019-09586-y.

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5

Shaik, Khaja Moinuddin, Kumar M. Pradeep, Kumar G. Sandeep, Ramya Perugumi, Sravya Sree Konda, and K. Kavya. "A review on micro beads: Formulation, technological aspects, and extraction." GSC Biological and Pharmaceutical Sciences 26, no. 2 (2024): 059–66. https://doi.org/10.5281/zenodo.10969852.

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Any drug delivery system's purpose is to deliver a therapeutic amount of medicine to the appropriate place in the body while also achieving and maintaining the correct drug concentration. This could be accomplished by using numerous unit dosage forms such as microgranules/spheroids, pellets, microcapsules, and beads, which are divided into many separate units, referred to as subunits, each of which possesses certain desired features. The advantages of micro particle drug delivery systems over single unit dose form are well documented. One of the solutions that does not entail the use of harsh
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6

Jaradat, Abdolelah, Ali Alazzo, Mohammad F. Bayan, and Wasfy Obeidat. "A Green, Solvent- and Cation-Free Approach for Preparing 5-Fluorouracil-Loaded Alginate Nanoparticles Using Microfluidic Technology." Pharmaceutics 17, no. 4 (2025): 438. https://doi.org/10.3390/pharmaceutics17040438.

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Background/Objectives: Alginate nanoparticles (NPs) are commonly synthesised using either an emulsion technique that involves organic solvent use or ionotropic gelation utilising multivalent cations, e.g., Ca+2. However, the extensive use of organic solvents imposes detrimental effects on the ecosystem, and using multivalent cations as crosslinkers could eventually lead to the leakage of these cations, thus disrupting nanoparticle matrices. Therefore, this study aimed to overcome the limitations of these techniques by eliminating the usage of organic solvents and multivalent cations. Methods:
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7

Chebout, Afaf, Makhlouf Chaalal, Siham Ydjedd, and Louiza Himed. "Optimization of Malabar Nut (Justicia adhatoda L.) Leaves’ Phenolic Compounds by Alginate Emulsion-gelation Approach using Response Surface Methodology." Current Bioactive Compounds 20 (March 12, 2024). http://dx.doi.org/10.2174/0115734072297243240304113132.

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Background: The encapsulation technique is an effective method for coating bioactive molecules and protecting them against various technological treatment conditions during production processing. Objective: The aim of this study was to optimize the encapsulation conditions of phenolic compounds extracted from Malabar nut (Justicia adhatoda L.) leaves by alginate emulsion-gelation approach using response surface methodology Methods: The ionotropic gelation method was used to encapsulate the phenolic compounds of Malabar nut (Justicia adhatoda L.) leaves. The optimization of this phenolic compou
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8

Saleh, Noha, Soha Elshaer, and Germeen Girgis. "Biodegradable polymers-based nanoparticles to enhance the antifungal efficacy of fluconazole against Candida albicans." Current Pharmaceutical Biotechnology 22 (July 8, 2021). http://dx.doi.org/10.2174/1389201022666210708105142.

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Background: Fluconazole (FLZ), a potent antifungal medication, is characterized by poor water solubility that reduced its antifungal efficacy. Objective: This study aimed to prepare FLZ-loaded polymeric nanoparticles (NPs) by using different polymers and techniques as a mean of enhancing the antifungal activity of FLZ. Methods: NP1, NP2, and NP3 were prepared by the double emulsion/solvent evaporation method using PLGA, PCL, and PLA, respectively. The ionotropic pre-gelation technique was applied to prepare an alginate/chitosan-based formulation (NP4). Particle size, zeta potential, encapsulat
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Hema, Naga Durga Divvela*1 Lohithasu Duppala2 Srikavya Nelapudi1. "FORMULATION DEVELOPMENT AND EVALUATION OF OILENTRAPPED FLOATING ALGINATE BEADS OF RANITIDINE HYDROCHLORIDE FOR SUSTAINED RELEASE." June 30, 2018. https://doi.org/10.5281/zenodo.2531142.

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The present investigation deals with the preparation and evaluation of oilentrapped floating alginate beads of Ranitidine hydrochloride for sustained release. The beads were prepared by ionotropic emulsion-gelation method. The prepared beads were evaluated for percentage yield, entrapment efficiency, micromeretic studies, in-vitro drug release studies, stability studies. Ranitidine hydrochloride floating beads which are prepared with polymers such as polyvinyl pyrrolidone (PVP) and hydroxyethyl cellulose (HEC), were free flowing and showed almost spherical shape. The beads showed excellent flo
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10

Samal, Himansu Bhusan, Itishree Jogmaya Das, Sabina Yasmin, et al. "Formulate Lornoxicam Bio Adhesive Microspheres Using Different Polymers by Ionotropic Gelation Method and Emulsion Cross Linking Method: An Integrated Molecular Dynamics Approach." Journal of Pharmaceutical Innovation 20, no. 1 (2025). https://doi.org/10.1007/s12247-024-09895-x.

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