Morphology and release profile of microcapsules encapsulating peppermint oil by complex coacervation

2011 ◽  
Vol 104 (3) ◽  
pp. 455-460 ◽  
Author(s):  
Zhijian Dong ◽  
Yong Ma ◽  
Khizar Hayat ◽  
Chengsheng Jia ◽  
Shuqin Xia ◽  
...  
2019 ◽  
Vol 87 ◽  
pp. 71-82 ◽  
Author(s):  
Michele Cristina Rodrigues da Cruz ◽  
João Luiz Andreotti Dagostin ◽  
Camila Augusto Perussello ◽  
Maria Lúcia Masson

2012 ◽  
Vol 602-604 ◽  
pp. 1285-1288
Author(s):  
Dan Wang ◽  
De Fu Chi

The chitosan-gum arabic microcapsules prepared by complex coacervation were chosen as carrier for a model insect semiochemicals, α-pinene, owing non-toxicity of the polymers and mild conditions of the method. The coated colloids were characterized using scanning electron microscopy (SEM). The release of α-pinene from microspheres was studied in simulated conditions. The results showed that α-pinene-loaded microspheres which were obtained by association had a mean diameter of 5±0.5µm. The encapsulation efficiency and the encapsulation yield of the α-pinene-loaded microspheres were about 51.70±2.5% and 42.11±2.3%, respectively. The release experiments revealed that polyelectrolytes prolonged the release time of the encapsulated α-pinene. The release rate of α-pinene from the microspheres was proportional to the release time.


2021 ◽  
Vol 11 (9) ◽  
pp. 3956
Author(s):  
Wilhelm Robert Glomm ◽  
Peter Patrick Molesworth ◽  
Eugenia Mariana Sandru ◽  
Le Thuy Truong ◽  
Anders Brunsvik ◽  
...  

Most liquid food flavours such as essential oils are volatile and prone to degradation in the presence of oxygen, light, moisture and high temperatures. Microencapsulation of volatile ingredients prior to use in food or beverages is a commonly used process to limit loss and degradation of flavours and aromas during processing and storage. Here, peppermint essential oil was microencapsulated via complex coacervation using a combination of bovine serum albumin and gum Acacia as wall materials. The resulting core-shell microcapsules were chemically crosslinked with a modified food-grade starch, and subsequently spray dried, resulting in dry microcapsules which could be easily redispersed in aqueous solutions. Microcapsule formation and stability, as well as microencapsulation yield of peppermint oil, were investigated as a function of polymer concentration, core material load/wall thickness and crosslinker concentration. The crosslinked peppermint oil microcapsules were spherical and mononuclear both before and after spray drying and redispersion, whereas control coacervate samples without crosslinker did not withstand the spray drying process. Microencapsulation yield as analysed by GC-MS showed no loss of peppermint oil during or after complex coacervation, and 54% loss after spray drying for the best combination of Polymer:Oil ratio and crosslinker concentration used here, indicating good overall protection of the core material.


2019 ◽  
Vol 9 (01) ◽  
pp. 58-64
Author(s):  
Senthilnathan B ◽  
Billy Graham R ◽  
Chaarmila Sherin C ◽  
Vivekanandan K ◽  
Bhavya E

Objective: Drug targeting is the capacity of the dosage form. In which the therapeutic agent acts specifically to desired site of action in the non-targeted tissue with the help of Nano particles is called as the drug targeting. IMATINIB is a used to treat cancer by chemo therapy. Cancers like chronic myeloid leukemia cancer (CML) and acute lymphoblastic leukemia cancer (ALL) and other specific types of gastrointestinal stromal cell tumor (GIST) systemic mast cell disease and Bone marrow failure disorder. It is administered by oral root. For ATP, Tyrosine kinase is act as a binding site. Methodology: The drug IMATINIB is loaded in the polymer chitosan, poly-(D) glucosamine is a bio compactible, bio degradable, nontoxic, antimicrobial and soluble in solvents. This preparation is done by emulsion-droplet coalescence method. Content of the Drug, Size of the particle and Zeta potential, Encapsulation efficiency and Drug release testing are described for this formulation in this study. Results: The Imatinib Nano particles were formulated and evaluated for its invitro drug release profile. Based on the invitro drug release profile of Imatinib nano particles formulation (INP1 – INP5) formulation INP3 was selected as the best formulation in which the particle size was 285.9nm. The invitro % drug release of INP3 formulation was 99.76 ± 0.82 and it was found to be the suitable formulation to manage the cancer. Conclusion: Hence it is concluded that the newly formulated controlled release nanoparticle drug delivery system of Imatinib may be idol and effective by allowing the drug to release continuously for 24 hrs.


Author(s):  
Rajesh Dubey ◽  
Udaya K. Chowdary ◽  
Venkateswarlu V.

A controlled release formulation of metoclopramide was developed using a combination of hypromellose (HPMC) and hydrogenated castor oil (HCO). Developed formulations released the drug over 20 hr with release kinetics following Higuchi model. Compared to HCO, HPMC showed significantly higher influence in controlling the drug release at initial as well as later phase. The difference in the influence can be explained by the different swelling and erosion behaviour of the polymers. Effect of the polymers on release was optimized using a face-centered central composite design to generate a predictable design space. Statistical analysis of the drug release at various levels indicated a linear effect of the polymers’ levels on the drug release. The release profile of formulations containing the polymer levels at extremes of their ranges in design space was found to be similar to the predicted release profile


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