Propofol in anesthesia. mechanism of action, structure-activity relationships, and drug delivery

被引:292
|
作者
Trapani, G
Altomare, C
Sanna, E
Biggio, G
Liso, G
机构
[1] Univ Bari, Fac Farm, Dipartimento Farmacochim, I-70125 Bari, Italy
[2] Univ Cagliari, Sez Neurosci, Dipartimento Biol Sperimentale, Monserrato, CA, Italy
关键词
D O I
10.2174/0929867003375335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Propofol (2,6-diisopropylphenol) is becoming the intravenous anesthetic of choice for ambulatory surgery in outpatients. It is extensively metabolized, with most of the administered dose appearing in the urine as glucuronide conjugates. Favorable operating conditions and rapid recovery are claimed as the main advantages in using propofol, whereas disadvantages include a relatively high incidence of apnea, and blood pressure reductions. Besides a literature summary of the pharmacodynamics, pharmacokinetics, toxicology, and clinical use, this review provides a deeper discussion on the current understanding of mechanism of action and structure-activity relationships, and recent findings on drug delivery technologies as applied to the improvement of propofol formulations. The action of propofol involves a positive modulation of the inhibitory function of the neurotransmitter gamma-aminobutyric acid (GABA) through GABA(A) receptors. Recent results from recombinant human GABAA receptor experiments and findings from the work exploring the effects at other receptors (e.g., glycine, nicotinic, and M1 muscarinic receptors) are reviewed. Studies showing its antiepileptic and anxiolytic properties are also discussed. The structure-activity relationships (SAR) of series of alkylphenols and p-X-substituted congeners have been reinvestigated. Interestingly, unlike the other congeners tested sofar, p-iodo-2,6-diisopropylphenol displayed anticonvulsant and anticonflict effects, but not sedative-hypnotic and anesthetic properties. Due to its high lipid-solubility, propofol was initially formulated as a solution with the surfactant Cremophor EL, but the occurrence of pain on injection and anaphylactoid reactions prompted to search for alternative formulations. Results from using cyclodextrins, water-soluble prodrugs, and adopting Bodor's approach to the site-specific chemical delivery system (CDS), as well as the advantages provided by computer-controlled infusion systems, are examined in some detail.
引用
收藏
页码:249 / 271
页数:23
相关论文
共 50 条
  • [1] Structure-activity relationships and cellular mechanism of action of small molecules that enhance the delivery of oligonucleotides
    Juliano, Rudolph L.
    Wang, Ling
    Tavares, Francis
    Brown, Edward G.
    James, Lindsey
    Ariyarathna, Yamuna
    Ming, Xin
    Mao, Chengqiong
    Suto, Mark
    NUCLEIC ACIDS RESEARCH, 2018, 46 (04) : 1601 - 1613
  • [2] Structure-activity relationships for Pimephales and Tetrahymena: A mechanism of action approach
    Bearden, AP
    Schultz, TW
    ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 1997, 16 (06) : 1311 - 1317
  • [3] Structure-Activity Relationships and Drug Allergy
    Hasdenteufel, Frederic
    Luyasu, Samuel
    Hougardy, Nicolas
    Fisher, Malcolm
    Boisbrun, Michel
    Mertes, Paul-Michel
    Kanny, Gisele
    CURRENT CLINICAL PHARMACOLOGY, 2012, 7 (01): : 15 - 27
  • [4] Towards establishing structure-activity relationships for mesoporous silica in drug delivery applications
    Rosenholm, Jessica M.
    Linden, Mika
    JOURNAL OF CONTROLLED RELEASE, 2008, 128 (02) : 157 - 164
  • [5] DDS - MECHANISMS OF ACTION AND STRUCTURE-ACTIVITY RELATIONSHIPS
    VANDYKE, K
    ARCHIVES INTERNATIONALES DE PHARMACODYNAMIE ET DE THERAPIE, 1972, 200 (01): : 147 - +
  • [6] Phellinus linteus polysaccharides: A review on their preparation, structure-activity relationships, and drug delivery systems
    Kou, Fang
    Mei, Yuxia
    Wang, Weihao
    Wei, Xuetuan
    Xiao, Hang
    Wu, Xian
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2024, 258
  • [7] Structure-Activity Relationships and Mechanism of Action of Macrolides Derived from Erythromycin as Antibacterial Agents
    Liang, Jian-Hua
    Han, Xu
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2013, 13 (24) : 3131 - 3164
  • [8] Photodynamic action of hypocrellin dyes: structure-activity relationships
    He, YY
    Liu, HY
    An, JY
    Han, R
    Jiang, LJ
    DYES AND PIGMENTS, 1999, 44 (01) : 63 - 67
  • [9] Exploring Structure-Activity Relationships and Modes of Action of Laterocidine
    Thombare, Varsha J.
    Swarbrick, James D.
    Azad, Mohammad A. K.
    Zhu, Yan
    Lu, Jing
    Yu, Heidi Y.
    Wickremasinghe, Hasini
    He, Xiaoji
    Bandiatmakur, Mahimna
    Li, Rong
    Bergen, Phillip J.
    Velkov, Tony
    Wang, Jiping
    Roberts, Kade D.
    Li, Jian
    Patil, Nitin A.
    ACS CENTRAL SCIENCE, 2024, 10 (09) : 1703 - 1717
  • [10] Structure-Activity Relationship of Supramolecular Compounds in Drug Delivery
    Alakshmi, P. Raj
    Peter, Daniel N.
    Johnson, Jesu S.
    Ananthi, Nallamuthu
    MINI-REVIEWS IN ORGANIC CHEMISTRY, 2021, 18 (07) : 961 - 989