High-Loading Self-Assembling Peptide Nanoparticles as a Lipid-Free Carrier for Hydrophobic General Anesthetics

References

• Gong ZY, Liu XY, Dong JH, et al. Transition from vesicles to nanofibres in the enzymatic self-assemblies of an amphiphilic peptide as an antitumour drug carrier. Nanoscale. 2019;11(33):15479–15486. doi:10.1039/C9NR02874A
   PubMedGoogle Scholar
• Wang Q, Jiang N, Fu B, Huang F, Liu JF. Self-assembling peptide-based nanodrug delivery systems. Biomater Sci. 2019;7(12):4888–4911. doi:10.1039/C9BM01212E
   PubMed Web of Science ®Google Scholar
• Peng F, Zhang WS, Qiu F. Self-assembling peptides in current nanomedicine: versatile nanomaterials for drug delivery. Curr Med Chem. 2020;27(29):4855–4881. doi:10.2174/0929867326666190712154021
   PubMedGoogle Scholar
• Fatouros DG, Lamprou DA, Urquhart AJ, et al. Lipid-like self-assembling peptide nanovesicles for drug delivery. ACS Appl Mater Interfaces. 2014;6(11):8184–8189. doi:10.1021/am501673x
   PubMedGoogle Scholar
• Chen YZ, Tang CK, Zhang J, Gong M, Su B, Qiu F. Self-assembling surfactant-like peptide A6K as potential delivery system for hydrophobic drugs. Int J Nanomedicine. 2015;10:847–858. doi:10.2147/IJN.S71696
   PubMed Web of Science ®Google Scholar
• Chan KH, Tay JJJ. Advancement of peptide nanobiotechnology via emerging microfluidic technology. Micromachines (Basel). 2019;10:627. doi:10.3390/mi10100627
   PubMed Web of Science ®Google Scholar
• Meng C, Wei WP, Wang YH, et al. Study of the interaction between self-assembling peptide and mangiferin and in vitro release of mangiferin from in situ hydrogel. Int J Nanomedicine. 2019;14:7447–7460. doi:10.2147/IJN.S208267
   PubMed Web of Science ®Google Scholar
• Briuglia ML, Urquhart AJ, Lamprou DA. Sustained and controlled release of lipophilic drugs from a self-assembling amphiphilic peptide hydrogel. Int J Pharm. 2014;474(1–2):103–111. doi:10.1016/j.ijpharm.2014.08.025
   PubMedGoogle Scholar
• Ishida A, Watanabe G, Oshikawa M, Ajioka I, Muraoka T. Glycine substitution effects on the supramolecular morphology and rigidity of cell-adhesive amphiphilic peptides. Chemistry. 2019;25(59):13523–13530. doi:10.1002/chem.201902083
   PubMedGoogle Scholar
• Paul S, Kumari K, Paul S. Molecular insight into the effects of enhanced hydrophobicity on amyloid-like aggregation. J Phys Chem B. 2020;124(45):10048–10061. doi:10.1021/acs.jpcb.0c06000
   PubMedGoogle Scholar
• Chen YZ, Xing ZH, Liao DQ, Qiu F. Neglected hydrophobicity of dimethanediyl group in peptide self-assembly: a hint from amyloid-like peptide GNNQQNY and its derivatives. J Phys Chem B. 2018;122(46):10470–10477. doi:10.1021/acs.jpcb.8b09220
   PubMedGoogle Scholar
• Gu XL, Qiu M, Sun HL, et al. Polytyrosine nanoparticles enable ultra-high loading of doxorubicin and rapid enzyme-responsive drug release. Biomater Sci. 2018;6(6):1526–1534. doi:10.1039/C8BM00243F
   PubMedGoogle Scholar
• Costache AD, Sheihet L, Zaveri K, Knight DD, Kohn J. Polymer-drug interactions in tyrosine-derived triblock copolymer nanospheres: a computational modeling approach. Mol Pharm. 2009;6(5):1620–1627. doi:10.1021/mp900114w
   PubMed Web of Science ®Google Scholar
• Sheihet L, Piotrowska K, Dubin RA, Kohn J, Devore D. Effect of tyrosine-derived triblock copolymer compositions on nanosphere self-assembly and drug delivery. Biomacromolecules. 2007;8(3):998–1003. doi:10.1021/bm060860t
   PubMedGoogle Scholar
• Ravenelle F, Gori S, Le Garrec D, et al. Novel lipid and preservative-free propofol formulation: properties and pharmacodynamics. Pharm Res. 2008;25(2):313–319. doi:10.1007/s11095-007-9471-5
   PubMedGoogle Scholar
• Noble RMN, Salim SY, Walker B, et al. Survival of staphylococcus epidermidis in propofol and intralipid in the dead space of intravenous injection ports. Anesth Analg. 2019;129(1):e20–e22. doi:10.1213/ANE.0000000000002654
   PubMedGoogle Scholar
• Devlin JW, Lau AK, Tanios MA. Propofol-associated hypertriglyceridemia and pancreatitis in the intensive care unit: an analysis of frequency and risk factors. Pharmacotherapy. 2005;25(10):1348–1352. doi:10.1592/phco.2005.25.10.1348
   PubMedGoogle Scholar
• Devaud JC, Berger MM, Pannatier A, et al. Hypertriglyceridemia: a potential side effect of propofol sedation in critical illness. Intensive Care Med. 2012;38(12):1990–1998. doi:10.1007/s00134-012-2688-8
   PubMed Web of Science ®Google Scholar
• Rodrigues TA, Alexandrino RA, Kanczuk ME, Gozzani JL, Mathias LA. A comparative study of non-lipid nanoemulsion of propofol with solutol and propofol emulsion with lecithin. Rev Bras Anestesiol. 2012;62(3):325–334. doi:10.1016/S0034-7094(12)70133-2
   PubMedGoogle Scholar
• Krajčová A, Waldauf P, Anděl M, Duška F. Propofol infusion syndrome: a structured review of experimental studies and 153 published case reports. Crit Care. 2015;19(1):398. doi:10.1186/s13054-015-1112-5
   PubMedGoogle Scholar
• Zhou Y, Yang J, Liu J, Wang Y, Zhang WS. Efficacy comparison of the novel water-soluble propofol prodrug HX0969w and fospropofol in mice and rats. Br J Anaesth. 2013;111(5):825–832. doi:10.1093/bja/aet218
   PubMedGoogle Scholar
• Deng T, Mao XL, Li Y, Bo SW, Yang ZG, Jiang ZX. Monodisperse oligoethylene glycols modified Propofol prodrugs. Bioorg Med Chem Lett. 2018;28(22):3502–3505. doi:10.1016/j.bmcl.2018.10.009
   PubMedGoogle Scholar
• Ravenelle F, Vachon P, Rigby-Jones AE, et al. Anaesthetic effects of propofol polymeric micelle: a novel water soluble propofol formulation. Br J Anaesth. 2008;101(2):186–193. doi:10.1093/bja/aen147
   PubMed Web of Science ®Google Scholar
• Boscan P, Rezende ML, Grimsrud K, Stanley SD, Mama KR, Steffey EP. Pharmacokinetic profile in relation to anaesthesia characteristics after a 5% micellar microemulsion of propofol in the horse. Br J Anaesth. 2010;104(3):330–337. doi:10.1093/bja/aep377
   PubMedGoogle Scholar
• Wu AL, Wang YY, Min S, Liu H, Xie F. Etomidate-loaded micelles for short-acting general anesthesia: preparation, characterizations, and in vivo studies. J Drug Deliv Sci Technol. 2018;46:156–161. doi:10.1016/j.jddst.2018.05.013
   Web of Science ®Google Scholar
• Wang B, Chen SM, Yang J, Yang LH, Liu J, Zhang WS. ET-26 hydrochloride (ET-26 HCl) has similar hemodynamic stability to that of etomidate in normal and uncontrolled hemorrhagic shock (UHS) rats. PLoS One. 2017;12(8):e0183439. doi:10.1371/journal.pone.0183439
   PubMedGoogle Scholar
• Wang B, Yang J, Chen J, et al. An etomidate analogue with less adrenocortical suppression, stable hemodynamics, and improved behavioral recovery in rats. Anesth Analg. 2017;125(2):442–450. doi:10.1213/ANE.0000000000002063
   PubMed Web of Science ®Google Scholar
• National Research Council Committee for the Update of the Guide for the C, Use of Laboratory A. The National Academies Collection: Reports Funded by National Institutes of Health. Guide for the Care and Use of Laboratory Animals. Washington (DC): National Academies Press (US); 2011. Copyright © 2011, National Academy of Sciences. doi:10.17226/12910
   Google Scholar
• Dickinson R, White I, Lieb WR, Franks NP. Stereoselective loss of righting reflex in rats by isoflurane. Anesthesiology. 2000;93(3):837–843. doi:10.1097/00000542-200009000-00035
   PubMedGoogle Scholar
• Kilpatrick GJ, McIntyre MS, Cox RF, et al. CNS 7056: a novel ultra-short-acting benzodiazepine. Anesthesiology. 2007;107(1):60–66. doi:10.1097/01.anes.0000267503.85085.c0
   PubMed Web of Science ®Google Scholar
• Dixon WJ. Staircase bioassay: the up-and-down method. Neurosci Biobehav Rev. 1991;15(1):47–50. doi:10.1016/S0149-7634(05)80090-9
   PubMed Web of Science ®Google Scholar
• Lee JM, Park KM, Lim SJ, Lee MK, Kim CK. Microemulsion formulation of clonixic acid: solubility enhancement and pain reduction. J Pharm Pharmacol. 2002;54(1):43–49. doi:10.1211/0022357021771904
   PubMedGoogle Scholar
• Date AA, Nagarsenker MS. Design and evaluation of microemulsions for improved parenteral delivery of propofol. AAPS PharmSciTech. 2008;9(1):138–145. doi:10.1208/s12249-007-9023-7
   PubMed Web of Science ®Google Scholar
• Cotten JF, Husain SS, Forman SA, et al. Methoxycarbonyl-etomidate: a novel rapidly metabolized and ultra-short-acting etomidate analogue that does not produce prolonged adrenocortical suppression. Anesthesiology. 2009;111(2):240–249. doi:10.1097/ALN.0b013e3181ae63d1
   PubMed Web of Science ®Google Scholar
• Li X, Zhang Y, Fan Y, et al. Preparation and evaluation of novel mixed micelles as nanocarriers for intravenous delivery of propofol. Nanoscale Res Lett. 2011;6(1):275. doi:10.1186/1556-276X-6-275
   PubMedGoogle Scholar
• Doenicke A, Roizen MF, Hoernecke R, Mayer M, Ostwald P, Foss J. Haemolysis after etomidate: comparison of propylene glycol and lipid formulations. Br J Anaesth. 1997;79(3):386–388. doi:10.1093/bja/79.3.386
   PubMed Web of Science ®Google Scholar
• Doenicke AW, Roizen MF, Hoernecke R, Lorenz W, Ostwald P. Solvent for etomidate may cause pain and adverse effects. Br J Anaesth. 1999;83(3):464–466. doi:10.1093/bja/83.3.464
   PubMedGoogle Scholar
• Nakane M, Iwama H. A potential mechanism of propofol-induced pain on injection based on studies using nafamostat mesilate. Br J Anaesth. 1999;83(3):397–404. doi:10.1093/bja/83.3.397
   PubMedGoogle Scholar
• Gehan G, Karoubi P, Quinet F, Leroy A, Rathat C, Pourriat JL. Optimal dose of lignocaine for preventing pain on injection of propofol. Br J Anaesth. 1991;66(3):324–326. doi:10.1093/bja/66.3.324
   PubMedGoogle Scholar
• Shimizu T, Inomata S, Kihara S, Toyooka H, Brimacombe JR. Rapid injection reduces pain on injection with propofol. Eur J Anaesthesiol. 2005;22(5):394–396. doi:10.1017/S0265021505230673
   PubMedGoogle Scholar
• Park JW, Park ES, Chi SC, Kil HY, Lee KH. The effect of lidocaine on the globule size distribution of propofol emulsions. Anesth Analg. 2003;97(3):769–771. doi:10.1213/01.ANE.0000074797.70349.CA
   PubMed Web of Science ®Google Scholar
• Li GL, Fan YT, Li XR, et al. In vitro and in vivo evaluation of a simple microemulsion formulation for propofol. Int J Pharm. 2012;425(1–2):53–61. doi:10.1016/j.ijpharm.2012.01.011
   PubMedGoogle Scholar
• Chan KH, Lee WH, Ni M, Loo Y, Hauser CAE. C-terminal residue of ultrashort peptides impacts on molecular self-assembly, hydrogelation, and interaction with small-molecule drugs. Sci Rep. 2018;8(1):17127. doi:10.1038/s41598-018-35431-2
   PubMed Web of Science ®Google Scholar