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Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer. / Roy, Biplab; Guha, Pritam; Chang, Chien-Hsiang ; Nahak, Prasant; Karmakar, Gourab; Быков, Алексей Геннадьевич; Акентьев, Александр Владимирович; Носков, Борис Анатольевич; Patra, Anuttam; Dutta, Kunal; Ghosh, Chandradipa ; Panda, Amiya Kumar.

In: Chemistry and Physics of Lipids, Vol. 258, 10364, 01.01.2024.

Research output: Contribution to journalArticlepeer-review

Harvard

Roy, B, Guha, P, Chang, C-H, Nahak, P, Karmakar, G, Быков, АГ, Акентьев, АВ, Носков, БА, Patra, A, Dutta, K, Ghosh, C & Panda, AK 2024, 'Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer', Chemistry and Physics of Lipids, vol. 258, 10364. https://doi.org/10.1016/j.chemphyslip.2023.105364

APA

Roy, B., Guha, P., Chang, C-H., Nahak, P., Karmakar, G., Быков, А. Г., Акентьев, А. В., Носков, Б. А., Patra, A., Dutta, K., Ghosh, C., & Panda, A. K. (2024). Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer. Chemistry and Physics of Lipids, 258, [10364]. https://doi.org/10.1016/j.chemphyslip.2023.105364

Vancouver

Roy B, Guha P, Chang C-H, Nahak P, Karmakar G, Быков АГ et al. Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer. Chemistry and Physics of Lipids. 2024 Jan 1;258. 10364. https://doi.org/10.1016/j.chemphyslip.2023.105364

Author

Roy, Biplab ; Guha, Pritam ; Chang, Chien-Hsiang ; Nahak, Prasant ; Karmakar, Gourab ; Быков, Алексей Геннадьевич ; Акентьев, Александр Владимирович ; Носков, Борис Анатольевич ; Patra, Anuttam ; Dutta, Kunal ; Ghosh, Chandradipa ; Panda, Amiya Kumar. / Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer. In: Chemistry and Physics of Lipids. 2024 ; Vol. 258.

BibTeX

@article{94775280f6254c3d9f2c4b0a281ca79e,
title = "Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer",
abstract = "Interactions between a zwitterionic phospholipid, 1, 2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and four anionic phospholipids dihexadecyl phosphate (DHP), 1, 2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG), 1, 2-dipalmitoyl-sn-glycero-3-phosphate (DPP) and 1, 2-dipalmitoyl-sn-glycero-3-phospho ethanol (DPPEth) in combination with an additional amount of 30 mol% cholesterol were separately investigated at air-buffer interface through surface pressure (π) - area (A) measurements. π-A isotherm derived parameters revealed maximum negative deviation from ideality for the mixtures comprising 30 mol% anionic lipids. Besides the film functionality, structural changes of the monomolecular films at different surface pressures in the absence and presence of polyamidoamine (PAMAM, generation 4), a cationic dendrimer, were visualised through Brewster angle microscopy and fluorescence microscopic studies. Fluidity/rigidity of monolayers were assessed by surface dilatational rheology studies. Effect of PAMAM on the formation of adsorbed monolayer, due to bilayer disintegration of liposomes (DPPC:anionic lipids= 7:3 M/M, and 30 mol% cholesterol) were monitored by surface pressure (π) - time (t) isotherms. Bilayer disintegration kinetics were dependent on lipid head group and chain length, besides dendrimer concentration. Such studies are considered to be an in vitro cell membrane model where the alteration of molecular orientation play important roles in understanding the nature of interaction between the dendrimer and cell membrane. Liposome-dendrimer aggregates were nontoxic to breast cancer cell line as well as in doxorubicin treated MDA-MB-468 cell line suggesting their potential as drug delivery systems.",
keywords = "Langmuir monolayer, Bilayer disintegration, PAMAM-dendrimer, Bilayer disintegration, Langmuir monolayer, PAMAM-dendrimer",
author = "Biplab Roy and Pritam Guha and Chien-Hsiang Chang and Prasant Nahak and Gourab Karmakar and Быков, {Алексей Геннадьевич} and Акентьев, {Александр Владимирович} and Носков, {Борис Анатольевич} and Anuttam Patra and Kunal Dutta and Chandradipa Ghosh and Panda, {Amiya Kumar}",
year = "2024",
month = jan,
day = "1",
doi = "10.1016/j.chemphyslip.2023.105364",
language = "English",
volume = "258",
journal = "Chemistry and Physics of Lipids",
issn = "0009-3084",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Effect of cationic dendrimer on membrane mimetic systems in the form of monolayer and bilayer

AU - Roy, Biplab

AU - Guha, Pritam

AU - Chang, Chien-Hsiang

AU - Nahak, Prasant

AU - Karmakar, Gourab

AU - Быков, Алексей Геннадьевич

AU - Акентьев, Александр Владимирович

AU - Носков, Борис Анатольевич

AU - Patra, Anuttam

AU - Dutta, Kunal

AU - Ghosh, Chandradipa

AU - Panda, Amiya Kumar

PY - 2024/1/1

Y1 - 2024/1/1

N2 - Interactions between a zwitterionic phospholipid, 1, 2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and four anionic phospholipids dihexadecyl phosphate (DHP), 1, 2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG), 1, 2-dipalmitoyl-sn-glycero-3-phosphate (DPP) and 1, 2-dipalmitoyl-sn-glycero-3-phospho ethanol (DPPEth) in combination with an additional amount of 30 mol% cholesterol were separately investigated at air-buffer interface through surface pressure (π) - area (A) measurements. π-A isotherm derived parameters revealed maximum negative deviation from ideality for the mixtures comprising 30 mol% anionic lipids. Besides the film functionality, structural changes of the monomolecular films at different surface pressures in the absence and presence of polyamidoamine (PAMAM, generation 4), a cationic dendrimer, were visualised through Brewster angle microscopy and fluorescence microscopic studies. Fluidity/rigidity of monolayers were assessed by surface dilatational rheology studies. Effect of PAMAM on the formation of adsorbed monolayer, due to bilayer disintegration of liposomes (DPPC:anionic lipids= 7:3 M/M, and 30 mol% cholesterol) were monitored by surface pressure (π) - time (t) isotherms. Bilayer disintegration kinetics were dependent on lipid head group and chain length, besides dendrimer concentration. Such studies are considered to be an in vitro cell membrane model where the alteration of molecular orientation play important roles in understanding the nature of interaction between the dendrimer and cell membrane. Liposome-dendrimer aggregates were nontoxic to breast cancer cell line as well as in doxorubicin treated MDA-MB-468 cell line suggesting their potential as drug delivery systems.

AB - Interactions between a zwitterionic phospholipid, 1, 2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and four anionic phospholipids dihexadecyl phosphate (DHP), 1, 2-dimyristoyl-sn-glycero-3-phosphoglycerol (DMPG), 1, 2-dipalmitoyl-sn-glycero-3-phosphate (DPP) and 1, 2-dipalmitoyl-sn-glycero-3-phospho ethanol (DPPEth) in combination with an additional amount of 30 mol% cholesterol were separately investigated at air-buffer interface through surface pressure (π) - area (A) measurements. π-A isotherm derived parameters revealed maximum negative deviation from ideality for the mixtures comprising 30 mol% anionic lipids. Besides the film functionality, structural changes of the monomolecular films at different surface pressures in the absence and presence of polyamidoamine (PAMAM, generation 4), a cationic dendrimer, were visualised through Brewster angle microscopy and fluorescence microscopic studies. Fluidity/rigidity of monolayers were assessed by surface dilatational rheology studies. Effect of PAMAM on the formation of adsorbed monolayer, due to bilayer disintegration of liposomes (DPPC:anionic lipids= 7:3 M/M, and 30 mol% cholesterol) were monitored by surface pressure (π) - time (t) isotherms. Bilayer disintegration kinetics were dependent on lipid head group and chain length, besides dendrimer concentration. Such studies are considered to be an in vitro cell membrane model where the alteration of molecular orientation play important roles in understanding the nature of interaction between the dendrimer and cell membrane. Liposome-dendrimer aggregates were nontoxic to breast cancer cell line as well as in doxorubicin treated MDA-MB-468 cell line suggesting their potential as drug delivery systems.

KW - Langmuir monolayer

KW - Bilayer disintegration

KW - PAMAM-dendrimer

KW - Bilayer disintegration

KW - Langmuir monolayer

KW - PAMAM-dendrimer

UR - https://www.mendeley.com/catalogue/72d4b97c-fbee-3bc9-b2b3-c638c9070968/

U2 - 10.1016/j.chemphyslip.2023.105364

DO - 10.1016/j.chemphyslip.2023.105364

M3 - Article

VL - 258

JO - Chemistry and Physics of Lipids

JF - Chemistry and Physics of Lipids

SN - 0009-3084

M1 - 10364

ER -

ID: 114899731