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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974568/
Hoshino K, Kimura T, De Grand AM, et al. Three catheter-based strategies for cardiac delivery of therapeutic gelatin microspheres. Gene Ther. 2006; 13 (18):1320–1327. Liang HC, Chang WH, Lin KJ, et al. Genipin-crosslinked gelatin microspheres as a drug carrier for intramuscular administration: in vitro and in vivo studies.Author: Luis Solorio, Christopher Zwolinski, Amanda W. Lund, Megan J. Farrell, Jan P. Stegemann, Jan P. Steg...
https://www.ncbi.nlm.nih.gov/pubmed/17763059
Gelatin microspheres cross-linked with EDC as a drug delivery system for doxycyline: development and characterization. Adhirajan N(1), Shanmugasundaram N, Babu M. Author information: (1)Biomaterials Division, Central Leather Research Institute, Chennai, Tamil Nadu, India.Author: N. Adhirajan, N. Shanmugasundaram, Mary Babu
https://www.ijpsonline.com/articles/biodegradable-gelatin-microspheres-as-controlled-release-intraarticular-delivery-system-the-effect-of-formulation-variab.pdf
Farhangi, et al.: Gelatin Microspheres for Intraarticular Delivery Intraarticular administration of microspheres containing non-steroidal antiinflammatory drugs is beneficial in the treatment of rheumatoid arthritis. Microspheres could localize drug at the site of administrationAuthor: M. Farhangi, S. Dadashzadeh, N. Bolourchian
https://www.sciencedirect.com/science/article/pii/S0168365904000331
Therefore, it can be concluded that the gelatin microspheres treated with microwave energy appear to be suitable as drug delivery system for the drug administration. Gelatin microspheres microwave-treated at 250 °C for 10 min can be easily loaded by the soaking process, avoiding the most likely drug degradation produced by the high temperature ...Author: Maria Angela Vandelli, Marcello Romagnoli, Alessandra Monti, Manuela Gozzi, Paolo Guerra, Francesco ...
https://www.ijpsonline.com/articles/biodegradable-gelatin-microspheres-as-controlled-release-intraarticular-delivery-system-the-effect-of-formulation-variables.html
May 26, 2016 · Biodegradable Gelatin Microspheres as Controlled Release Intraarticular Delivery System: The Effect of Formulation Variables, M. Farhangi, S. Dadashzadeh and N. Bolourchian*Author: M. Farhangi, S. Dadashzadeh, N. Bolourchian
https://www.sciencedirect.com/science/article/pii/S0378517300006815
The biocompatibility studies showed that the microspheres crosslinked with GAL are well tolerated in vivo. These results suggest the potential application of gelatin microspheres crosslinked with GAL as a suitable drug delivery system for the subcutaneous administration.Author: Maria Angela Vandelli, Francesco Rivasi, P. Guerra, Flavio Forni, R. Arletti
https://www.hindawi.com/journals/ijbm/2014/829490/
Information on the preparation and properties of starch/gelatin blend microparticles with and without crosslinking for drug delivery is presented. The blend microparticles were prepared by the water-in-oil emulsion solvent diffusion method. Glutaraldehyde and methylene blue were used as the crosslinker and the water-soluble drug model, respectively. The blend microparticles were characterized ...Author: Theeraphol Phromsopha, Yodthong Baimark
https://www.jgtps.com/admin/uploads/YqxI0h.pdf
usually formulated into microspheres and filling them into hard gelatin capsules. Microspheres received much attention not only for prolonged release, but also for targeting of drugs. In future microspheres will find the central place in novel drug delivery, particularly …
https://www.cancer.gov/publications/dictionaries/cancer-drug/def/tris-acryl-gelatin-microspheres
An embolic particle composed of water-soluble, compressible, nonabsorbable tris-acryl gelatin microspheres, with potential use for embolization. Upon administration, the tris-acryl gelatin microspheres (TAGM) serve as an embolic agent before surgery for highly vascularized areas, such as those seen in certain tumors, by penetrating into the vascular system and blocking blood flow.
https://www.tandfonline.com/doi/pdf/10.3109/10717544.2011.595842
The purpose of the study is to design and evaluate curcumin loaded gelatin microspheres (C-GMS) for effective drug delivery to the lung. C-GMS was prepared by the emulsification-linkage technique and the formulation was optimized by orthogonal design. The mean encapsulation efficiency and drug loading of the optimal C-GMS were
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