Relevant bibliographies by topics / Polylactic-co-glycolic acid

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Polylactic-co-glycolic acid'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Polylactic-co-glycolic acid"

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Liu, Liping, Jing Tan, Baoyuan Li, et al. "Construction of functional pancreatic artificial islet tissue composed of fibroblast-modified polylactic-co-glycolic acid membrane and pancreatic stem cells." Journal of Biomaterials Applications 32, no. 3 (2017): 362–72. http://dx.doi.org/10.1177/0885328217722041.

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Objective To improve the biocompatibility between polylactic- co-glycolic acid membrane and pancreatic stem cells, rat fibroblasts were used to modify the polylactic- co-glycolic acid membrane. Meanwhile, we constructed artificial islet tissue by compound culturing the pancreatic stem cells and the fibroblast-modified polylactic- co-glycolic acid membrane and explored the function of artificial islets in diabetic nude mice. Methods Pancreatic stem cells were cultured on the fibroblast-modified polylactic- co-glycolic acid membrane in dulbecco's modified eagle medium containing activin-A, β-cat
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Yammine, Paolo, Rima Kassab, and Dima Moussa. "Encapsulation of an antifungal agent within biodegradable polymers: composition effect." JOURNAL OF ADVANCES IN CHEMISTRY 12, no. 3 (2016): 4274–79. http://dx.doi.org/10.24297/jac.v12i3.2168.

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Polylactic acid and poly(lactic-co-glycolic acid) are two aliphatic polyesters commonly used in drug delivery systems. Having a hydrophobic nature, they could be used for the encapsulation of hydrophobic drugs such as Amphotericin B. Drug-loaded microspheres were prepared using solvent evaporation by changing the ratio of Polylactic acid to poly(lactic-co-glycolic acid) in the organic mixture. Results showed that higher drug encapsulation and drug loading values were seen for formulations having higher lactide content. This had also influenced the drug release rate which was slower at higher l
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Tazhbayev, Burkeyev, Zhaparova, Zhumagalieva, and Arystanova. "Nanoparticles on the basis of polylactic acid and polylactic-co-glycolic acids loaded with drugs." Bulletin of the Karaganda University. "Chemistry" series 90, no. 2 (2018): 31–39. http://dx.doi.org/10.31489/2018ch2/31-39.

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Branton, Alice, Mahendra Kumar Trivedi, Dahryn Trivedi, Gopal Nayak, and Snehasis Jana. "Physicochemical and Thermal Characterization of Biofield Energy Treated Polylactic-co-glycolic acid (PLGA)." Journal of Analytical, Bioanalytical and Separation Techniques 4, no. 1 (2019): 1–6. https://doi.org/10.15436/2476-1869.19.2026.

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Polylactic-co-glycolic acid (PLGA) is a biodegradable copolymer. It has many applications in the pharmaceuticals and biomedical industries, but its degradation and stability is a major concern. The objective of this study was to evaluate the influence of the Trivedi Effect® on the physicochemical and thermal properties of PLGA using modern analytical techniques. The PLGA sample was divided into control and Biofield Energy Treated parts. The control sample did not obtain the Biofield Energy Treatment, whereas the treated PLGA was received the Trivedi Effect®-Consciousness Energy Healing
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Ariyasu, Kazumasa, Atsuhiro Ishii, Taiga Umemoto, and Mitsuhiro Terakawa. "Laser-triggered release of encapsulated molecules from polylactic-co-glycolic acid microcapsules." Journal of Biomedical Optics 21, no. 8 (2016): 085003. http://dx.doi.org/10.1117/1.jbo.21.8.085003.

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Safaei, Mohsen, Farnoosh Khaleseh, Saba Ahmadi, et al. "Antibacterial effect of polylactic-co-glycolic acid/selenium nanocomposite against dental biofilm." Polimery 70, no. 3 (2025): 186–93. https://doi.org/10.14314/polimery.2025.3.4.

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To determine the optimal conditions for obtaining poly(lactic-co-glycolic) acid with selenium (PLGA/selenium) nanocomposites the Taguchi method was used. FT-IR, Raman spectroscopy, XRD and FESEM analysis confirmed the nanocomposites’ structure. The nanocomposite containing 6 mg/mL of selenium obtained in the process where the mixing time was 75 min showed the highest antibacterial activity against Streptococcus mutans. The obtained nanocomposites are an innovative approach to improving oral health and can be used as antibacterial materials for medical and dental applications.
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Pradhan, Roshan, Bijay Kumar Poudel, Thiruganesh Ramasamy, Han-Gon Choi, Chul Soon Yong, and Jong Oh Kim. "Docetaxel-Loaded Polylactic Acid-Co-Glycolic Acid Nanoparticles: Formulation, Physicochemical Characterization and Cytotoxicity Studies." Journal of Nanoscience and Nanotechnology 13, no. 8 (2013): 5948–56. http://dx.doi.org/10.1166/jnn.2013.7735.

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Kaval, Berna, Fatma Dilara Şen, Kemal Kaya Batmaz, Meliha Ekinci, and A. Alper Öztürk. "Latest research about active pharmaceutical ingredient loaded Poly Lactic Acid-co-Glycolic Acid (PLGA) based drug delivery system in Türkiye." European Journal of Life Sciences 1, no. 3 (2023): 127–39. http://dx.doi.org/10.55971/ejls.1197082.

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Some of the most well-engineered and produced biomaterials are polyesters based on polyglycolic acid (PGA), polylactic acid (PLA), and their copolymers, polylactic acid co-glycolic acid (PLGA). In controlled release systems, PLGA is the most extensively used and popular polymer. Because of its biodegradability, biocompatibility, and favorable release kinetics, but also because of the reliability of protein delivery issues, this synthetic polymer has been found to be very successful. PLGA is approved in various human drug delivery systems by EMA and FDA. In this review, first, PLGA and historic
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Contreras-Magallanes, Yesenia Guadalupe, Marina Durán-Aguilar, Susana L. Sosa-Gallegos, et al. "Prime Vaccination with Chitosan-Coated Phipps BCG and Boosting with CFP-PLGA against Tuberculosis in a Goat Model." Animals 11, no. 4 (2021): 1046. http://dx.doi.org/10.3390/ani11041046.

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Attempts to improve the immune response and efficacy of vaccines against tuberculosis in cattle, goats, and other animal species have been the focus of research in this field during the last two decades. Improving the vaccine efficacy is essential prior to running long-lasting and expensive field trials. Studies have shown that vaccine protocols utilizing boosting with proteins improve the vaccine efficacy. The use of polymers such as chitosan and PolyLactic-co-Glycolic Acid (PLGA) improves the immune response against different diseases by improving the interaction of antigens with the cellula
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Jiang, Jun, Jianpeng Xiao, Dongqing Wang, and Huazhong Cai. "Application of Implantable Polylactic-Co-Glycolic Acid Microcapsule in Repairing Alveolar Bone Defects." Evidence-Based Complementary and Alternative Medicine 2021 (July 27, 2021): 1–10. http://dx.doi.org/10.1155/2021/5580785.

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Alveolar bone defects (ABDs) were a perennial problem, especially in the aged. Bisphosphonates, especially etidronate sodium (ET), were frequently used in clinical treatment of ABD. However, the oral administration of ET had poor absorption (<1%). Therefore, optimization of a suitable dosage form substituted with ET to locally repair the ABD was a straightforward approach. Polylactide-co-glycolide (PLGA) is a biodegradable material and had been used in locally implanted medical devices. Therefore, an ET-PLGA microcapsule may help local delivery and prolong the activity of healing ABD. In th
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Dissertations / Theses on the topic "Polylactic-co-glycolic acid"

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Booysen, Laetitia Lucretia Ismarelda Josephine. "The in vitro and in vivo pharmacokinetic parameters of polylactic-co-glycolic acid nanoparticles encapsulating anti-tuberculosis drugs / L.L.I.J. Booysen." Thesis, North-West University, 2012. http://hdl.handle.net/10394/9106.

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Tuberculosis (TB) is an infectious, deadly disease, caused by Mycobacterium tuberculosis (M.tb). In 2010, there were 8,8 million incident cases of TB globally. South Africa currently has the third highest TB incident cases worldwide. In an attempt to address the challenges facing TB chemotherapy, among which frequent dosing and long duration of therapy resulting in poor patient compliance, a novel poly(DL-lactic-co-glycolic) acid (PLGA) nanoparticulate drug delivery system (DDS) encapsulating anti-TB drugs was developed. It is hypothesised that this nanoparticulate DDS will address the challen
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Guegan, Eric. "Transport characteristics using nor-dihydroguaiaretic acid (NDGA)-polymerized collagen fibers as a local drug delivery system." [Tampa, Fla.] : University of South Florida, 2007. http://purl.fcla.edu/usf/dc/et/SFE0002042.

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Jasti, Bhaskara Rao. "Characterization of polymorphic forms and in vitro release of etoposide from poly-DL-lactic and poly-DL-lactic-co-glycolic acid micromatrices." Scholarly Commons, 1995. https://scholarlycommons.pacific.edu/uop_etds/2654.

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Etoposide has been shown to be effective in the treatment of testicular and small-cell lung cancers, lymphoma, leukemia and Kaposi's sarcoma. Several clinical investigations have suggested that the prolonged maintenance of greater than 1 $\mu$g/ml concentration in plasma would provide better therapeutic response in patients. Thus use of a sustained/controlled release formulation of etoposide was indicated. This investigation focused on the potential for the development of a sustained/controlled release dosage form of etoposide for a 7-15 day delivery using selected polylactic and polylactic-co
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Book chapters on the topic "Polylactic-co-glycolic acid"

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Avgoustakis, Konstantinos. "Polylactic-Co-Glycolic Acid (PLGA)." In Encyclopedia of Biomaterials and Biomedical Engineering, Second Edition - Four Volume Set. CRC Press, 2008. http://dx.doi.org/10.1201/b18990-216.

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"Polylactic-Co-Glycolic Acid (PLGA)." In Encyclopedia of Biomaterials and Biomedical Engineering, Second Edition. CRC Press, 2008. http://dx.doi.org/10.1081/e-ebbe2-120013950.

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Avgoustakis, Konstantinos. "Polylactic-co-Glycolic Acid (PLGA)." In Encyclopedia of Biomedical Polymers and Polymeric Biomaterials. Taylor & Francis, 2016. http://dx.doi.org/10.1081/e-ebpp-120013950.

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"Polylactic-Co-Glycolic Acid (PLGA) / Konstantinos Avgoustakis." In Encyclopedia of Biomaterials and Biomedical Engineering. CRC Press, 2008. http://dx.doi.org/10.1201/9780429154065-216.

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Chavda, Vivek P., Pankti C. Balar, Rajashri Bezbaruah, Dixa A. Vaghela, and Krupa Vyas. "Theranostics polylactic-co-glycolic acid nanoparticles mediated drug delivery." In Theranostics Nanomaterials in Drug Delivery. Elsevier, 2025. http://dx.doi.org/10.1016/b978-0-443-22044-9.00006-1.

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Cobongela, S. Z. Z. "Polymers in Drug Delivery." In Materials Research Foundations. Materials Research Forum LLC, 2025. https://doi.org/10.21741/9781644903353-11.

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Polymers are crucial in drug delivery systems (DDS), enhancing the efficacy and safety of therapeutics through controlled release, targeted delivery, and improved bioavailability. Natural polymers like alginate and chitosan offer biocompatibility and biodegradability, while synthetic polymers such as polyethylene glycol (PEG) and polylactic-co-glycolic acid (PLGA) provide solubility and controlled release. The incorporation of nanotechnology with polymers has led to advanced nanocarriers, enhancing drug stability and therapeutic effectiveness. Despite challenges like potential toxicity and com
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Nazemiyeh, Amirreza, Niloufar Ahdeno, Hamed Dadashi, et al. "Electrospinning of Nanocellulose–Synthetic Polymer Composites: A Multifaceted Approach to Tissue Engineering Breakthroughs." In Nanocellulose-based Hybrid Systems for Tissue Engineering. Royal Society of Chemistry, 2024. https://doi.org/10.1039/9781837673094-00151.

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Nanocellulose, an abundant and versatile natural polymer, has garnered significant attention in the field of tissue engineering (TE) due to its remarkable properties, including biocompatibility, biodegradability, high surface area, and mechanical strength. This chapter provides an in-depth overview of the combination of nanocellulose with various synthetic polymers, such as polyesters, polyanhydrides, polyurethanes, and polyacrylic acid, to create advanced composite materials for TE applications. The chapter also delves into the unique characteristics and advantages of each polymer class when
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Conference papers on the topic "Polylactic-co-glycolic acid"

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Mulia, Kamarza, Dwiantari Satyapertiwi, Ranee Devina, and Elsa Krisanti. "Characterization of polylactic co-glycolic acid nanospheres modified with PVA and DDAB." In BIOMEDICAL ENGINEERING’S RECENT PROGRESS IN BIOMATERIALS, DRUGS DEVELOPMENT, AND MEDICAL DEVICES: Proceedings of the First International Symposium of Biomedical Engineering (ISBE 2016). Author(s), 2017. http://dx.doi.org/10.1063/1.4976767.

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Gul-e-Saba, A. Adulphakdee, A. Madthing, M. N. Zafar, and M. A. Abdullah. "Modeling of hyaluronic acid containing anti-cancer drugs-loaded polylactic-co-glycolic acid bioconjugates for targeted delivery to cancer cells." In INTERNATIONAL CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCES 2012: (ICFAS2012). AIP, 2012. http://dx.doi.org/10.1063/1.4757441.

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Subhash, Hrebesh M., Hui Xie, Jeffrey W. Smith, and Owen McCarty. "Optical characterization and feasibility study of multifunctional polylactic-co-glycolic acid (PLGA) nanoparticles designed for photo-thermal optical coherence tomography." In European Conference on Biomedical Optics. OSA, 2011. http://dx.doi.org/10.1364/ecbo.2011.809108.

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Subhash, Hrebesh M., Hui Xie, Jeffrey W. Smith, and Owen McCarty. "Optical characterization and feasibility study of multifunctional polylactic-co-glycolic acid (PLGA) nanoparticles designed for photo-thermal optical coherence tomography." In European Conferences on Biomedical Optics, edited by Rainer A. Leitgeb and Brett E. Bouma. SPIE, 2011. http://dx.doi.org/10.1117/12.889760.

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Muthuswamy, Prabhahar, Prakash Sekar, Saravana Kumar Magalingam, and Vivek Rai. "Surface treatment by wire electric discharge machining of Ti–6Al–4V alloy and polylactic co-glycolic acid (PLGA) coated plates using RSM technologies." In BIOPOLYMER, SMART MATERIALS AND ENGINEERING MATERIALS. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0194010.

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Guegan, Eric, Tian Davis, Thomas J. Koob, and Yvonne Moussy. "Transport Characteristics of a Novel Local Drug Delivery System Using Nordihydroguaiaretic Acid (NDGA)-Polymerized Collagen Fibers." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-171428.

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Local delivery of a drug in vivo would permit high interstitial drug concentration at the desired location without producing high systemic drug levels. Previous local drug delivery systems have included biodegradable polymer implants, hydrogels, and osmotic pumps [1]. In this paper, we describe a novel local drug delivery system using nordihydroguaiaretic acid (NDGA)-polymerized collagen fibers. NDGA collagen fibers were originally developed for use as biocompatible tendon bioprostheses [2]. The NDGA collagen fibers were loaded with either: dexamethasone, a synthetic glucocorticoid with anti-i
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