Bibliografias temáticas / Lactams

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Literatura científica selecionada sobre o tema "Lactams"

Autor: Grafiati

Publicado: 4 de junho de 2021

Última modificação: 25 de julho de 2025

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Artigos de revistas sobre o assunto "Lactams"

Li, Lu, Qiyao Wang, Hui Zhang, Minjun Yang, Mazhar I. Khan та Xiaohui Zhou. "Sensor histidine kinase is a β-lactam receptor and induces resistance to β-lactam antibiotics". Proceedings of the National Academy of Sciences 113, № 6 (2016): 1648–53. http://dx.doi.org/10.1073/pnas.1520300113.

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β-Lactams disrupt bacterial cell wall synthesis, and these agents are the most widely used antibiotics. One of the principle mechanisms by which bacteria resist the action of β-lactams is by producing β-lactamases, enzymes that degrade β-lactams. In Gram-negative bacteria, production of β-lactamases is often induced in response to the antibiotic-associated damage to the cell wall. Here, we have identified a previously unidentified mechanism that governs β-lactamase production. In the Gram-negative enteric pathogenVibrio parahaemolyticus, we found a histidine kinase/response regulator pair (Vbr

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Medina, Marjorie B., Dana J. Poole та M. Ranae Anderson. "A Screening Method for β-Lactams in Tissues Hydrolyzed with Penicillinase I and Lactamase II". Journal of AOAC INTERNATIONAL 81, № 5 (1998): 963–72. http://dx.doi.org/10.1093/jaoac/81.5.963.

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Abstract Antibiotic residues above tolerance levels are not allowed in foods derived from farm animals. Microbial inhibition assays are used to screen antibiotics in U.S. regulatory laboratories. We developed a screening approach to classify β-lactams through selective hydrolysis of the β-lactam ring with Penase™ or lactamase II, thereby inactivating the β- lactam activity. Optimum conditions for hydrolysis of β-lactams with Penase and lactamase II were determined. p-Lactams were detected by a microbial inhibition assay and with enzyme-linked immunosorbent assays before and after hydrolysis. β

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Alves, Américo J. S., Nuno G. Alves, Cátia C. Caratão, et al. "Spiro-Lactams as Novel Antimicrobial Agents." Current Topics in Medicinal Chemistry 20, no. 2 (2020): 140–52. http://dx.doi.org/10.2174/1568026619666191105110049.

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Introduction: Structural modulation of previously identified lead spiro-β-lactams with antimicrobial activity was carried out. Objective: The main objective of this work was to synthesize and evaluate the biological activity of novel spiro-lactams based on previously identified lead compounds with antimicrobial activity. Methods: The target chiral spiro-γ-lactams were synthesized through 1,3-dipolar cycloaddition reaction of a diazo-γ-lactam with electron-deficient dipolarophiles. In vitro activity against HIV and Plasmodium of a wide range of spiro-β-lactams and spiro-γ-lactams was evaluated.

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Li, Xian-Zhi, Li Zhang, Ramakrishnan Srikumar та Keith Poole. "β-Lactamase Inhibitors Are Substrates for the Multidrug Efflux Pumps of Pseudomonas aeruginosa". Antimicrobial Agents and Chemotherapy 42, № 2 (1998): 399–403. http://dx.doi.org/10.1128/aac.42.2.399.

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ABSTRACT The MexAB-OprM multidrug efflux system exports a number of antimicrobial compounds, including β-lactams. In an attempt to define more fully the range of antimicrobial compounds exported by this system, and, in particular, to determine whether β-lactamase inhibitors were also accommodated by the MexAB-OprM pump, the influence of pump status (its presence or absence) on the intrinsic antibacterial activities of these compounds and on their abilities to enhance β-lactam susceptibility in intact cells was assessed. MIC determinations clearly demonstrated that all three compounds tested, c

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Brilhante, R. S. N., L. G. A. Valente, M. F. G. Rocha та ін. "Sesquiterpene Farnesol Contributes to Increased Susceptibility to β-Lactams in Strains of Burkholderia pseudomallei". Antimicrobial Agents and Chemotherapy 56, № 4 (2012): 2198–200. http://dx.doi.org/10.1128/aac.05885-11.

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ABSTRACTThis study aimed to evaluate thein vitrocombination of farnesol and β-lactams againstBurkholderia pseudomallei. A total of 12 β-lactamase-positive strains were tested according to CLSI standards. All strains were inhibited by farnesol, with MICs ranging from 75 to 150 μM. The combination of this compound with β-lactams resulted in statistically significant β-lactam MIC reduction (P≤ 0.05). This study provides new perspectives for the use of farnesol combined with β-lactam antibiotics against strains ofB. pseudomallei.

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Jacobs, Lian M. C., Patrick Consol та Yu Chen. "Drug Discovery in the Field of β-Lactams: An Academic Perspective". Antibiotics 13, № 1 (2024): 59. http://dx.doi.org/10.3390/antibiotics13010059.

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β-Lactams are the most widely prescribed class of antibiotics that inhibit penicillin-binding proteins (PBPs), particularly transpeptidases that function in peptidoglycan synthesis. A major mechanism of antibiotic resistance is the production of β-lactamase enzymes, which are capable of hydrolyzing β-lactam antibiotics. There have been many efforts to counter increasing bacterial resistance against β-lactams. These studies have mainly focused on three areas: discovering novel inhibitors against β-lactamases, developing new β-lactams less susceptible to existing resistance mechanisms, and ident

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Sekiguchi, Jun-ichiro, Koji Morita, Tomoe Kitao та ін. "KHM-1, a Novel Plasmid-Mediated Metallo-β-Lactamase from a Citrobacter freundii Clinical Isolate". Antimicrobial Agents and Chemotherapy 52, № 11 (2008): 4194–97. http://dx.doi.org/10.1128/aac.01337-07.

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ABSTRACT A novel gene, bla KHM-1, encoding a metallo-β-lactamase, KHM-1, was cloned from a clinical isolate of Citrobacter freundii resistant to most β-lactam antibiotics. Escherichia coli expressing bla KHM-1 was resistant to all broad-spectrum β-lactams except for monobactams and showed reduced susceptibility to carbapenems. Recombinant KHM-1 exhibited EDTA-inhibitable hydrolytic activity against most β-lactams, with an overall preference for cephalosporins.

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Glen, Karl A., та Iain L. Lamont. "β-lactam Resistance in Pseudomonas aeruginosa: Current Status, Future Prospects". Pathogens 10, № 12 (2021): 1638. http://dx.doi.org/10.3390/pathogens10121638.

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Pseudomonas aeruginosa is a major opportunistic pathogen, causing a wide range of acute and chronic infections. β-lactam antibiotics including penicillins, carbapenems, monobactams, and cephalosporins play a key role in the treatment of P. aeruginosa infections. However, a significant number of isolates of these bacteria are resistant to β-lactams, complicating treatment of infections and leading to worse outcomes for patients. In this review, we summarize studies demonstrating the health and economic impacts associated with β-lactam-resistant P. aeruginosa. We then describe how β-lactams bind

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Mukhopadhyay, S., and P. Chakrabarti. "Altered permeability and beta-lactam resistance in a mutant of Mycobacterium smegmatis." Antimicrobial Agents and Chemotherapy 41, no. 8 (1997): 1721–24. http://dx.doi.org/10.1128/aac.41.8.1721.

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Beta-lactam resistance in mycobacteria results from an interplay between the following: (i) beta-lactamase production, (ii) affinity of the penicillin-binding proteins (PBPs) for the drugs, and (iii) permeation of the drugs. A laboratory mutant of Mycobacterium smegmatis was studied in order to evaluate the roles of these factors in beta-lactam resistance. Mutant M13 was between 7- and 78-fold more resistant than the wild type to cephaloridine, cefoxitin, cefazolin, cefamandole, and cephalothin. Increased beta-lactamase activity toward these antibiotics was not observed in the mutant. The PBP

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Li, Fu, Li Wan, Tongyang Xiao та ін. "In Vitro Activity of β-Lactams in Combination with β-Lactamase Inhibitors against Mycobacterium tuberculosis Clinical Isolates". BioMed Research International 2018 (2 липня 2018): 1–8. http://dx.doi.org/10.1155/2018/3579832.

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Objectives. Evaluating the activity of nineteen β-lactams in combination with different β-lactamase inhibitors to determine the most potent combination against Mycobacterium tuberculosis (MTB) in vitro. Methods. Drug activity was examined by drug susceptibility test with 122 clinical isolates from China. Mutations of blaC and drug targets ldtMt1, ldtMt2, dacB2, and crfA were analyzed by nucleotide sequencing. Results. Tebipenem (TBM) in combination with clavulanate (CLA) exhibited the highest anti-TB activity. The MIC of β-lactam antibiotics was reduced most evidently in the presence of CLA, c

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Teses / dissertações sobre o assunto "Lactams"

Betou, Marie. "Semipinacol rearrangement of cis-fused β-lactam diols into bicyclic lactams". Thesis, University of Birmingham, 2013. http://etheses.bham.ac.uk//id/eprint/4348/.

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The 6-azabicyclo[3.2.1]octane ring system is found in a wide variety of biologically active natural and non-natural products. The aim of this project is to prepare the 7,8-diketo-6-azabicyclo[3.2.1]octane structure via a semipinacol rearrangement of ring-fused β -lactams. Chapter 1 introduces the pinacol and semipinacol rearrangement, including the use of cyclic sulfites and phosphoranes, and ring expansion of β -lactams. Previous work in the Grainger group for the synthesis of lactams via tandem radical cyclisation-dithiocarbamate group transfer is also discussed. Chapter 2 describes the meth

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Warren, H. A. "New routes to sugar lactams, lactim ethers and cyclic amidines." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639351.

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Chapter 1 introduces the biological importance of glycosidase inhibitors. The biosynthesis of N-linked glycoproteins is briefly described and the mode of action of glycosidase enzymes is discussed. Some naturally occurring amino-sugar glycosidase inhibitors are detailed. In addition certain sugar lactones, lactams and cyclic amidines which have also been shown to inhibit glycosidase enzymes are reviewed. Chapter 2 introduces the syntheses of various polyhydroxylated piperidine and pyrrolidine alkaloids and sugar lactams. In addition the formation of cyclic sugar amidines and their derivatives

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Guignard, Guillaume Michel Pablo. "Open-chain building blocks from chiral lactams. Enantioselective synthesis of macrocyclic nitrogen-containing natural products." Doctoral thesis, Universitat de Barcelona, 2016. http://hdl.handle.net/10803/396650.

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1. (R)-Phenylglycinol-derived oxazolopiperidone lactams can be converted to enantiopure open-chain amino ester scaffolds by alkaline hydrolysis of the N-Boc 2-piperidones resulting from the reductive cleavage of the oxazolidine ring. 2. Lithium amidotrihydroborate (LiNH2BH3) reduction of diversely substituted (R)-phenylglycinol-derived oxazolopiperidone lactams brought about the reductive opening of both the oxazolidine and lactam rings, providing general access to structurally diverse enantiopure amino diols A bearing a variety of substitution patterns, substituents (alkyl, benzyl, aryl, p

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Sheppard, L. N. "Synthesis of B-lactams." Thesis, University of Oxford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.354855.

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McKenna, Jeffrey M. "Asymmetric synthesis of #beta#-lactams." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240681.

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Goh, Kee Chuan. "The biosynthesis of β-lactams". Thesis, University of Oxford, 1993. http://ora.ox.ac.uk/objects/uuid:24b6b29d-87cc-48f2-bd1b-bb64c663604f.

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This thesis reports the work done on two research projects which were carried out independently of each other but converge on the central theme of β-lactam biosynthesis. Chapter 1 provides an overview of biosynthesis in secondary metabolism, with special emphasis on current knowledge about the β-lactams. The first project, covered from Chapters 2 to 5, was part of our group's continuing effort to understand the structure and mechanism of Ring Expandase-Hydroxylase (REXH), an enzyme involved in the biosynthesis of cephalosporin C in Cephalosporium acremonium. REXH is a bifunctional enzyme, conv

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Welchman, Elizabeth Victoria. "The chemistry of Î² lactams." Thesis, University of Sunderland, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247775.

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Walker, Matthew David. "Diastereoselective reactions of atropisomeric lactams." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247569.

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Pearson, C. J. "Synthesis of aza-beta-lactams." Thesis, Imperial College London, 1985. http://hdl.handle.net/10044/1/37815.

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Joshi, S. N. "Diastereoselective synthesis of β-lactams". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2000. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2271.

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Mais fontes

Livros sobre o assunto "Lactams"

Ogliaruso, Michael A. Synthesis of lactones and lactams. Wiley, 1993.

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Bellido, F. The new -lactams: Mode of action, mechanisms of resistance. Roche, 1989.

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Banik, Bimal K., ed. Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5.

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Alcaide, B., and Bimal K. Banik. Heterocyclic scaffolds I: Ss-lactams. Springer, 2010.

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Janecki, Tomasz, ed. Natural Lactones and Lactams. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527666911.

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Hamao, Umezawa, Takeda Kagaku Shinkō Zaidan, and Takeda Science Foundation Symposium (4th : 1986 : Kyoto, Japan), eds. Frontiers of antibiotic research. Academic Press, 1987.

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Page, Michael I., ред. The Chemistry of β-Lactams. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2928-2.

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I, Page Michael, ed. The Chemistry of [beta]-lactams. Blackie Academic & Professional, 1992.

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Alle, Bruggink, ed. Synthesis of [beta]-lactam antibiotics: Chemistry, biocatalysis & process integration. Kluwer Academic Publishers, 2001.

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Ogliaruso, Michael A., and James F. Wolfe, eds. Synthesis of Lactones and Lactams (1993). John Wiley & Sons, Inc., 1993. http://dx.doi.org/10.1002/9780470772522.

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Capítulos de livros sobre o assunto "Lactams"

Singh, Girija S., and Siji Sudheesh. "β-Lactams." In Natural Lactones and Lactams. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527666911.ch3.

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Das, Aparna, and Bimal Krishna Banik. "Beta-Lactams." In Chemistry and Biology of Beta-Lactams. CRC Press, 2024. http://dx.doi.org/10.1201/9780367816339-1.

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Bhalla, Aman, Shamsher S. Bari, and Jitender Bhalla. "Synthesis of Diverse β-Lactams: Role of Appended Hetero Moiety on Its Activity." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_1.

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Sowinska, Marta, Maja Morawiak, Zofia Urbanczyk-Lipkowska, and Jolanta Solecka. "Nanochemistry in Drug Design." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_10.

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Palomo, Claudio, and Mikel Oiarbide. "Asymmetric Synthesis of β-Lactams via the Ketene-Imine Cycloaddition." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_11.

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Bhattacharya, Prabuddha, Sansa Dutta, Koushik Chandra, and Amit Basak. "The Never-Ending Story of β-Lactams: Use as Molecular Scaffolds and Building Blocks." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_12.

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Bari, Shamsher S., Aman Bhalla, and Jitender Bhalla. "Role of Transition Metal Reagents in β-Lactam Synthesis: New Paradigms." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_2.

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Klimczak, Urszula, Bartłomiej Furman, and Bartosz Zambroń. "4-Vinyloxyazetidin-2-one, a Novel Substrate for β-Lactam Synthesis." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_3.

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Tidwell, Thomas T. "β-Lactams from Ketene-Imine Cycloadditions: An Update." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_4.

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Delpiccolo, Carina M. L., Maitena Martinez-Amezaga, and Ernesto G. Mata. "Recent Approaches Toward the Generation of Molecular Diversity Based on β-Lactam Structures." In Beta-Lactams. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-55621-5_5.

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Trabalhos de conferências sobre o assunto "Lactams"

Padilla-Viveros, A. A., E. García-Ochoa, R. García-Esquivel, D. Alazard, M.-L. Fardeau, and B. Ollivier. "The Influence of the Culture Media on the Steel Corrosion Induced by Desulfovibrio vulgaris subsp. oxamicus: An Electrochemical Noise Study." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06522.

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Abstract The corrosion processes induced by Desulfovibrio vulgaris subsp. oxamicus (DSM192T) on carbon steel growing in lactate/sulfate and in lactate/nitrate media were analyzed through the use of electrochemical noise technique. Like some other sulfate-reducing bacteria, this Desulfovibrio species was able to reduce nitrate and produced ammonia in the absence of sulfate. Sterile control of lactate/sulfate culture medium without bacteria did not show any significant change in localization index (LI) evolution. However, the sterile control of lactate/nitrate culture medium showed the occurrenc

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Joseph, Jiya Mariya, Anjitha Harish, Jayakumar Rangasamy, and Reshmi R. "Optimization and Fabrication of Chitosan Lactate Nanofibrous Membrane." In 2025 2nd International Conference on Trends in Engineering Systems and Technologies (ICTEST). IEEE, 2025. https://doi.org/10.1109/ictest64710.2025.11042873.

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McLoughlin, Eavan, Niamh O'Boyle, and Mary Meegan. "Stories from Staudinger: Synthesis of chiral beta-lactams." In 5th International Electronic Conference on Medicinal Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06402.

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Kupka, Teobald, Piotr Lodowski, Maria Jaworska та Jan O. Dzięgielewski. "Semi empirical PM3 and spectroscopic studies on β-lactams". У The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47686.

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Espadinha, Margarida, Jorge Dourado, Rocio Lajarin-Cuesta, et al. "Bicyclic lactams as potential inhibitors of the NMDA receptor." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05631.

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McLoughlin, Eavan, та Niamh O'Boyle. "Enantiomeric β-Lactams for the Treatment of Breast Cancer". У 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07507.

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Couture, Axel, Pierre Grandclaudon, Stéphane Lebrun та Gwenaëlle Liberge. "Convenient synthesis of functionalized α-methylenebutano-4-lactams or lactones". У The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00570.

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Abood, Zeid Hassan, Amani Nadhim Kadhim та Husham Attallah Suhail. "Microwave assisted synthesis of new β-Lactams bearing thiadiazole moiety". У 4TH INTERNATIONAL SCIENTIFIC CONFERENCE OF ENGINEERING SCIENCES AND ADVANCES TECHNOLOGIES. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0157220.

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K. Alkhudhairy, Miaad, та Elhassan Benyagoub. "Frequency of Genes Mediated β-lactams Resistance in Acinetobacter Baumannii Isolates from Iraq". У X INTERNATIONAL CONGRESS OF PURE AND APPLIED TECHNOLOGICAL SCIENCES. Rimar Academy, 2023. http://dx.doi.org/10.47832/minarcongress10-2.

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Background: Acinetobacter baumannii is a nosocomial virulent microorganism that can cause acute and chronic infections in burn patients. The aim of the study: Diagnosis of genes mediated β-lactams resistance among test isolates. Materials and Methods: 649 swabs collected from inpatients with burn-wound infections at a burn center in Al-Najaf Province/ Iraq, from August 2022 to February 2023. Results: 68/ 649 (10.5%) isolates of Acinetobacter baumannii were identified according to microscopically, cultural, and biochemical features. 22 (32.4%) isolates were found able to produce extended-spectr

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Rezali, Nurul Syafiqah. "The Syntheses Of Fused Cyclic 5/6-Membered Ring Lactams Via Enamine Hydrogenation." In 8th International Conference on Multidisciplinary Research 2019. European Publisher, 2020. http://dx.doi.org/10.15405/epsbs.2020.03.03.87.

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Relatórios de organizações sobre o assunto "Lactams"

Cang, Huai Qin, XiangHua Quan, XiangHua Chu, Yu Liang, Xue Yang та Jing Li. Carbapenems versus β-lactam and β-lactamase inhibitors for treatment of Nosocomial Pneumonia: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.4.0113.

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Chiu, Chia-Yu, and Amara Sarwal. Impact of area under the curve-based vancomycin dosing combination with anti-pseudomonal beta-lactam antibiotics: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.12.0025.

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Review question / Objective: Did AUC-based vancomycin dosing reduce acute kidney injury than trough-based dosing when combined with anti-pseudomonal beta-lactam antibiotic? Condition being studied: Patients received Vancomycin combined with anti-pseudomonal beta-lactam antibiotics and monitor with either trough-base dosing or AUC-based dosing vancomycin. Information sources: All study types except case reports, case series, and conference abstracts were considered. PubMed, Embase, Cochrane Library, and ClinicalTrials.gov were searched from inception to November2022.

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Mosher, Jennifer J., Meghan M. Drake, Susan L. Carroll, et al. Microbial Community Dynamics of Lactate Enriched Hanford Groundwaters. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/986244.

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Meyer, Birte, and David Stahl. Syntrophic Degradation of Lactate in Methanogenic Co-cultures. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/986317.

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Ma, Lianjia. Multichannel Simultaneous Determination of Activities of Lactate Dehydrogenase. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/764689.

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Piper, Robert C. Parasite Lactate Dehydrogenase for Diagnosis of Plasmodium Falciparum. Phase II. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/adb230017.

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Li, Yuan, Benjamin Metcalf, Sopio Chochua та ін. Validation of β-lactam minimum inhibitory concentration predictions for pneumococcal isolates with newly encountered penicillin binding protein (PBP) sequences [Supporting data]. Centers for Disease Control and Prevention (U.S.), 2017. http://dx.doi.org/10.15620/cdc/147467.

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The datafiles, R scripts, MIC tables, and other files were used to evaluate the prediction performance of a penicillin-binding protein (PBP) typing system and two methods (Random Forest (RF) and Mode MIC (MM) previously developed by this research team. This data and these files support the finding of the paper "Validation of β-lactam minimum inhibitory concentration predictions for pneumococcal isolates with newly encountered penicillin binding protein (PBP) sequences" at https://doi.org/10.1186%2Fs12864-017-4017-7 or at https://stacks.cdc.gov/view/cdc/47684.

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Kim, Yuan, Edward M. Steadham, Steven M. Lonergan, and Elisabeth J. Huff-Lonergan. Antioxidant Capacity of Calcium Lactate on m-Calpain Activity In Vitro. Iowa State University, 2009. http://dx.doi.org/10.31274/ans_air-180814-1237.

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Reeves, John T. Beta-Adrenergic Blockade and Lactate Metabolism during Exercise at High Altitude. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada263544.

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ลีพิพัฒน์ไพบูลย์, ณัฐชนัญ, ธรรมนูญ หนูจักร, ศิริพัสตร์ ไชยันต์, ม.ล., ลักษณา ดูบาส та มนพิชา ศรีสะอาด. โครงการนำร่องการพัฒนาเทคนิคการตรวจวิเคราะห์สารเติมแต่ง สารปนเปื้อน สารตกค้าง สารสำคัญในอาหารและผลิตผลการเกษตร : รายงานการวิจัย. ภาควิชาเคมี คณะวิทยาศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2013. https://doi.org/10.58837/chula.res.2013.44.

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งานวิจัยนี้เป็นโครงงานวิจัยนำร่องสู่โครงการหลักมหาวิทยาลัยวิจัย คลัสเตอร์อาหารและน้ำหัวข้อการพัฒนาเทคนิคการตรวจวิเคราะห์สารเติมแต่ง สารปนเปื้อน สารตกค้าง สาระสำคัญในอาหารและผลิตผลการเกษตร นำเสนอการตรวจวัดสารยาสัตว์ตกค้างในเนื้อไก่การวิเคราะห์สารปนเปื้อนเหล่านี้ในสินค้าปศุสัตว์ทั้งสิ้น 24 ชนิด จาก 8 กลุ่มหลักได้แก่ กลุ่ม aminoglycosides 3 ชนิด, กลุ่ม β-lactam 3 ชนิด, กลุ่ม lincosamides 2 ชนิด, กลุ่ม macrolides 4 ชนิด, กลุ่ม quinolones 4 ชนิด, กลุ่ม sulfonamides 4 ชนิด, กลุ่ม tetracyclines 3 ชนิดและ amprollium โดยสกัดด้วยตัวทำละลายและวิเคราะห์ด้วยเทคนิคลิควิดโครมาโทกราฟีแทนเดมแมสสเปกโทรเมทรี โดย

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