References
- A. Villiers, “Sur la Fermentation de la Fécule Par l’action du Ferment Butyrique Comptes Rendus de l,” Académie des Sciences, no. 112 (1891): 536–8.
- R. Villalonga, R. Cao, and A. Fragoso, “Supramolecular Chemistry of Cyclodextrins in Enzyme Technology,” Chemical Reviews 107, no. 7 (2007): 3088–16.
- R. Breslo, and S. D. Dong, “Biomimetic Reactions Catalyzed by Cyclodextrins and Their Derivatives,” Chemical Reviews 98, no. 5 (1998): 1997–11.
- M. E. Davis, and M. E. Brewster, “Cyclodextrin-Based Pharmaceutics: Past, Present and Future,” Nature Reviews. Drug Discovery 3, no. 12 (2004): 1023–35.
- M. V. Rekharsky, and Y. Inoue, “Complexation Thermodynamics of Cyclodextrins,” Chemical Reviews 98, no. 5 (1998): 1875–18.
- T. Irie, and K. Uekama, “Pharmaceutical Applications of Cyclodextrins. III. Toxicological Issues and Safety Evaluation,” Journal of Pharmaceutical Sciences 86, no. 2 (1997): 147–62.
- E. Marttin, J. C. Verhoef, and F. W. Merkus, “Efficacy, Safety and Mechanism of Cyclodextrins as Absorption Enhancers in Nasal Delivery of Peptide and Protein Drugs,” Journal of Drug Targeting 6, no. 1 (1998): 17–36.
- C. B. Berde, and G. R. Strichartz, “Local Anesthetics,” Miller's Anesthesia 7, no. 7 (2010): 913–39.
- O. Galbes, A. Bourret, K. Nouette-Gaulain, F. Pillard, S. Matecki, G. Py, J. Mercier, X. Capdevila, and A. Philips, “N-Acetylcysteine Protects against Bupivacaine-Induced Myotoxicity Caused by Oxidative and Sarcoplasmic Reticulum Stress in Human Skeletal Myotubes,” Anesthesiology 113, no. 3 (2010): 560–9.
- S. L. Piper, and H. T. Kim, “Comparison of Ropivacaine and Bupivacaine Toxicity in Human Articular Chondrocytes,” The Journal of Bone and Joint Surgery 5, no. 90 (2008): 986–91.
- C. James, “Long-Term Consequences of Anesthetic Management,” Anesthesiology 1, no. 111 (2009): 1–4.
- H. Wada, S. Seki, T. Takahashi, N. Kawarabayashi, H. Higuchi, Y. Habu, S. Sugahara, and T. Kazama, “Combined Spinal and General Anesthesia Attenuates Liver Metastasis by Preserving TH1/TH2 Cytokine Balance,” Anesthesiology 106, no. 3 (2007): 499–06.
- K. Ogawa, M. Hirai, T. Katsube, M. Murayama, K. Hamaguchi, T. Shimakawa, Y. Naritake, T. Hosokawa, and T. Kajiwara, “Suppression of Cellular Immunity by Surgical Stress,” Surgery 127, no. 3 (2000): 329–36.
- H. Nagasaka, S. Ohno, K. Kobayashi, and H. Sakagami, “Effect of Anesthetics on Malignant Tumor Cells (a Review) 10,” Masui 10, no. 58 (2009): 1216–25.
- B. K. Ross, B. Coda, and C. H. Heath, “Local Anesthetic Distribution in a Spinal Model: A Possible Mechanism of Neurologic Injury after Continuous Spinal Anesthesia,” Regional Anaesthesia 2, no. 17 (1992): 69–77.
- T. Kishimoto, A. W. Bollen, and K. Drasner, “Comparative Spinal Neurotoxicity of Prilocaine and Lidocaine,” Anesthesiology 97, no. 5 (2002): 1250–3.
- T. Jonnesco, “ Remarks on General Spinal Analgesia,” British Medical Journal 2, no. 2550 (1909): 1396–401.
- A. W. Parr, D. E. Zoutman, and J. S. Davidson, “Antimicrobial Activity of Lidocaine against Bacteria Associated with Nosocomial Wound Infection,” Annals of Plastic Surgery 3, no. 43 (1999): 239–45.
- R. M. Schmidt, and H. S. Rosenkranz, “Antimicrobial Activity of Local Anaesthetics: Lidocaine and Procaine,” Journal of Infectious Diseases 121, no. 6 (1970): 597–12.
- W. Xing, D.-T. Chen, J.-H. Pan, Y.-H. Chen, Y. Yan, Q. Li, R.-F. Xue, Y.-F. Yuan, and W.-A. Zeng, “Lidocaine Induces Apoptosis and Suppresses Tumor Growth in Human Hepatocellular Carcinoma Cells in Vitro and in a Xenograft Model in Vivo,” Anesthesiology 126, no. 5 (2017): 868–81.
- M. Sakaguchi, Y. Kuroda, and M. Hirose, “The Antiproliferative Effect of Lidocaine on Human Tongue Cancer Cells with Inhibition of the Activity of Epidermal Growth Factor Receptor,” Anesthesia and Analgesia 102, no. 4 (2006): 1103–7.
- Y. Nishimura, Y. Miura, M. Maeda, H. Hayashi, M. Dong, H. Katsuyama, M. Tomita, F. Hyodoh, M. Kusaka, A. Uesaka, et.al, “Expression of the T Cell Receptor Vbeta repertoire in a human T cell resistant to asbestos-induced apoptosis and peripheral blood T cells from patients with silica and asbestos-related diseases ,” International Journal of Immunopathology and Pharmacology 19, no. 4 (2006): 795–05.
- S. Soni, and A. Pal, “Spectroscopic Studies on Host–Guest Interactions of α- and β-Cyclodextrin with Lidocaine Hydrochloride and Procaine Hydrochloride,” Journal of Solution Chemistry 45, no. 5 (2016): 665–74.
- V. R. Shaikh, S. S. Terdale, D. G. Hundiwale, and K. J. Patil, “Thermodynamic Studies of Drug–α-Cyclodextrin Interactions in Water at 298.15 K: Procaine Hydrochloride/Lidocaine Hydrochloride/Tetracaine Hydrochloride/Ranitidine Hydrochloride + α-Cyclodextrin + H2O Systems,” The Journal of Chemical Thermodynamics 68, no. 68 (2014): 161–8.
- A. Abou-Okeil, M. Rehan, S. M. El-Sawy, M. K. El-Bisi, O. A. Ahmed-Farid, and F. A. Abdel-Mohdy, “Lidocaine/β-Cyclodextrin Inclusion Complex as Drug Delivery System,” European Polymer Journal 108, no. 108 (2018): 304–10.
- L. Francisco, J. S. da Silva, F. A. do Carmo, V. R. de Almeida Borges, L. M. Monteiro, C. R. Rodrigues, L. M. Cabral, and V. P. de Sousa, “Preparation and Evaluation of Lidocaine Hydrochloride in Cyclodextrin Inclusion Complexes for Development of Stable Gel in Association with Chlorhexidine Gluconate for Urogenital Use,” International Journal of Nanomedicine 6, no. 6 (2011): 1143–54.
- R. Rajamohan, S. Kothai Nayaki, and M. Swaminathan, “Investigation on Association Behavior between 1-Aminoisoquinoline and β-Cyclodextrin in Solution and Solid State,” Journal of Molecular Liquids 220, no. 220 (2016): 918–25.