Towards an understanding of the release behavior of temperature-sensitive liposomes: a possible explanation of the "pseudoequilibrium'' release behavior at the phase transition temperature

被引:9
|
作者
Zhang, Xin [1 ]
Luckham, Paul F. [1 ]
Hughes, Alun D. [2 ]
Thom, Simon [2 ]
Xu, Xiao Yun [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Int Ctr Circulatory Hlth, Dept Clin Pharmacol, London, England
关键词
Lysolipid; mild-hyperthermia; release mechanism; thermal sensitive liposome; THERMOSENSITIVE LIPOSOMES; MILD HYPERTHERMIA; PERMEABILITY; DOXORUBICIN;
D O I
10.3109/08982104.2013.779702
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
It is generally believed that thermal sensitive liposomes (i.e. vesicles) that contain 1,2-dihexadecanoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine- N-[methoxy(polyethyleneglycol)-2000 (DSPE. 2000) maintain a constant permeability to ionic molecules when they are heated to the phase transition temperature of the membrane (T-m). However, DPPC: DSPE. 2000 liposome systems have been reported to release encapsulated agent in a "pseudoequilibrium'' pattern upon temperature rise, whereby there is a rapid release of encapsulated material followed by no further release. Little effort has been made to determine the mechanism of such release behavior. We aim to explore the potential cause of "pseudoequilibrium'' release of DPPC: DSPE. 2000 liposome systems in response to temperature rise. Using calcein as a hydrophilic marker, the release pattern of DPPC: DSPE. 2000 liposome system at T-m has been carefully determined. The potential mechanism of its release behavior has been further explored using two novel assays (i.e. heating-cooling-reheating assay and incubation assay). Our results show that there is a dramatic enhancement of the permeability of DPPC: DSPE. 2000 vesicles to ionized molecules (i.e. calcein) during the initial period of heating to 42 degrees C. This is believed to result from the opening of the hydrophilic pores at the liquid/solid interface. However, after less than 2 min of incubation at this temperature, no further release of calcein is observed, suggesting that the sizes of pores are reduced, restricting any further movement of calcein molecules. On cooling and reheating the DPPC: DSPE. 2000 liposomes to 42 degrees C, no further release of calcein is observed. The incorporation of MSPC (1-stearoyl-2-hydroxy-sn-glycero-3-phosphocholine) extends the release period of calcein from the DPPC: MSPC: DSPE. 2000 vesicles to more than 30 min, suggesting that the lysolipid stabilizes the pores in the lipid membrane.
引用
收藏
页码:167 / 173
页数:7
相关论文
共 21 条
  • [1] Formation of protein corona in vivo affects drug release from temperature-sensitive liposomes
    Al-Ahmady, Zahraa S.
    Hadjidemetriou, Marilena
    Gubbins, James
    Kostarelos, Kostas
    JOURNAL OF CONTROLLED RELEASE, 2018, 276 : 157 - 167
  • [2] In vitro Measurement of Release Kinetics of Temperature Sensitive Liposomes with a Fluorescence Imaging System
    Asemani, Davud
    Motamarry, Anjan
    Haemmerich, Dieter
    2018 40TH ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY (EMBC), 2018, : 3216 - 3219
  • [3] Temperature-sensitive polymers to promote heat-triggered drug release from liposomes: Towards bypassing EPR
    Amin, Mohamadreza
    Lammers, Twan
    ten Hagen, Timo L. M.
    ADVANCED DRUG DELIVERY REVIEWS, 2022, 189
  • [4] Encapsulated doxorubicin crystals influence lysolipid temperature-sensitive liposomes release and therapeutic efficacy in vitro and in vivo
    Ruiz, Amalia
    Ma, Guanglong
    Seitsonen, Jani
    Pereira, Sara G. T.
    Ruokolainen, Janne
    Al-Jamal, Wafa T.
    JOURNAL OF CONTROLLED RELEASE, 2020, 328 : 665 - 678
  • [5] Triggered Release of Doxorubicin from Temperature-Sensitive Poly(N-(2-hydroxypropyl)-methacrylamide mono/dilactate) Grafted Liposomes
    van Elk, Merel
    Deckers, Roel
    Oerlemans, Chris
    Shi, Yang
    Storm, Gert
    Vermonden, Tina
    Hennink, Wim E.
    BIOMACROMOLECULES, 2014, 15 (03) : 1002 - 1009
  • [6] Hyperthermia-triggered release of hypoxic cell radiosensitizers from temperature-sensitive liposomes improves radiotherapy efficacy in vitro
    Sadeghi, Negar
    Kok, Robbert Jan
    Bos, Clemens
    Zandvliet, Maurice
    Geerts, Willie J. C.
    Storm, Gert
    Moonen, Chrit T. W.
    Lammers, Twan
    Deckers, Roel
    NANOTECHNOLOGY, 2019, 30 (26)
  • [7] Drug release kinetics of temperature sensitive liposomes measured at high-temporal resolution with a millifluidic device
    Burke, Caitlin
    Dreher, Matthew R.
    Negussie, Ayele H.
    Mikhail, Andrew S.
    Yarmolenko, Pavel
    Patel, Aakash
    Skilskyj, Brenden
    Wood, Bradford J.
    Haemmerich, Dieter
    INTERNATIONAL JOURNAL OF HYPERTHERMIA, 2018, 34 (06) : 786 - 794
  • [8] Alginate microgels loaded with temperature sensitive liposomes for magnetic resonance imageable drug release and microgel visualization
    van Elk, Merel
    Lorenzato, Cyril
    Ozbakir, Burcin
    Oerlemans, Chris
    Storm, Gert
    Nijsen, Frank
    Deckers, Roel
    Vermonden, Tina
    Hennink, Wim E.
    EUROPEAN POLYMER JOURNAL, 2015, 72 : 620 - 631
  • [9] Physicochemical characteristics and doxorubicin-release behaviors of pH/temperature-sensitive polymeric nanoparticles
    Kang, SI
    Na, K
    Bae, YH
    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2003, 231 (1-3) : 103 - 112
  • [10] Near-Infrared Light Laser-Triggered Release of Doxorubicin and Sorafenib from Temperature-Sensitive Liposomes for Synergistic Therapy of Hepatocellular Carcinoma
    Peng, Yuan
    Su, Zhenwei
    Wang, Xin
    Wu, Teng
    Xiao, Hong
    Shuai, Xintao
    Lan, Yue
    JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2020, 16 (09) : 1381 - 1393