Publicado

2018-05-01

Structural analysis of adsorption processes of 5FU and imiquimodon hydrogels using AMBER/PM3 hybrid model

Análisis estructural de los procesos de adsorción de 5FU e imiquimod en hidrogeles utilizando el modelo híbrido AMBER/PM3

Análise estrutural de procedimentos de adsorção de 5FU e imiquimod em hidrogelas usando modelo híbrido AMBER/PM3

DOI:

https://doi.org/10.15446/rev.colomb.quim.v47n2.67352

Palabras clave:

5FU, Imiquimod, AMBER, PM3, FTIR, MESP, Gibbs (en)
5FU, Imiquimod, AMBER, PM3, FTIR, MESP, Gibbs (es)
5FU, Imiquimod, AMBER, PM3, FTIR, MESP, Gibbs (pt)

Autores/as

  • Norma Aurea Rangel-Vázquez INSTITUTO TECNOLOGICO DE AGAUSCALIENTES
  • Dulce Nallely Villanueva-García Instituto Tecnológico de Aguascalientes
  • Jonathan Kalla JK FP

AMBER/PM3 hybrid model allowed determining the structural properties of 5FU and imiquimod individually and after the adsorption of chitosan hydrogels crosslinked with genipin, respectively. It was observed that the Gibbs free energy (ΔG) decreases with the adsorption, but indicates thermodynamic stability and spontaneity in both processes; ΔG was verified by the increase in the dipole moments. On the one hand, the partition coefficient established the hydrophilic character with respect to the water present in the hydrogel, which increases with the adsorption. The FTIR showed that there were displacements in the signals, however, the hydrogen bond bands attributed to the formation of new bonds to perform the adsorption of the drugs were observed. The adsorption was verified by the MESP and the surface analysis, where the distribution of nucleophilic and electrophilic zone was observed.

El modelo hibrido AMBER/PM3permitió determinar las propiedades estructurales del 5FU e imiquimod individualmente y después de la adsorción en hidrogeles de quitosano entrecruzados con genipina, respectivamente. Se observó que la energía libre de Gibbs (ΔG) disminuye con la adsorción, sin embargo, en ambos procesos se encontró estabilidad termodinámica y espontaneidad; ΔG fue verificado mediante el incremento en los momentos dipolares. Por otro lado, el coeficiente de partición estableció el carácter hidrofìlico con respecto al agua presente en el hidrogel, el cual aumenta con la adsorción. El FTIR evidenció que existen desplazamientos en las señales. Se observaron las bandas de puente de hidrógeno, atribuidas a la formación de enlaces, para realizar la adsorción de los fármacos. La adsorción fue verificada mediante los MESP y los análisis de superficie, en donde se apreció la distribución de zonas nucleofílicas y electrofílicas.

O modelo hibrido AMBER/PM3 permitiu determinar as propriedades estruturadas do 5FU e imiquimod individualmente e depois da adsorção em hidrogeles de quitosano entrecruzados com genipina, respectivamente. Observou-se que o poder livre de Gibbs (ΔG) diminui com a adsorção, sem embargo, em ambos os processos se encontró estabilidade termodinâmica e espontaneidad; ΔG foi verificado através do aumento nos momentos de dipolares. Por outro lado, o coeficiente de divisão estabeleceu o carácter hidrofílico em relação à água presente no hidrogel, o qual aumenta com a adsorção. El FTIR evidenció que existem deslocamentos em las señales. Se observe as bandas de puente de hidrógeno, atribuições à formação de enlaces, para realizar a adsorção dos fármacos. A adsorção foi verificada através do MESP e os análises de superfície, em donde se apreciou a distribuição de zonas nucleofílicas e eletrofílicas.

Referencias

Fortina, P.; Kricka, L. J.; Surrey, S.; Grodzinski, P. Nanobiotechnology: the promise and reality of new approaches to molecular recognition. TrendsBiotechnol. 2006, 23, 168-173. DOI: https://doi.org/10.1016/j.tibtech.2005.02.007.

Sáez, V.; Hernáez, E.; Sanz-Angulo, L. Sistemas de liberación controlada de medicamentos. Rev. Iberoamer. Polím. 2002, 3, 1-20.

Nuñez, R.;Jáuregui-Haza, U. J. Las nanopartículas como portadores de fármacos: características y perspectivas. Revista CENIC. 2012, 43.

Lohcharoenka, W.; Wang, L.; Chen, Y. C.; Rojanasakul, Y. Protein nanoparticles as drug delivery carriers for cancer therapy. BioMed Research International.2014, 2014, 1-12. DOI: https://doi.org/10.1155/2014/180549.

Orthaber, K.; Pristovnik, M.; Skok, K.; Peric, B.; Maver, U. Skin cancer and its treatment: novel treatment approaches with emphasis on nanotechnology. J. Nanomaterials. 2017, 2017, 1-20. DOI: https://doi.org/10.1155/2017/2606271.

Chen, J.; Shao, R.; Zhang, X. D.; Chen, C. Applications of nanotechnology for melanoma treatment, diagnosis, and theranostics. International Journal of Nanomedicine. 2013, 8, 2677–2688. DOI: https://doi.org/10.2147/IJN.S45429.

Ganji, F.; Vasheghani-Farahani, S.; Vasheghani-Farahani, E. Theoretical description of hydrogel swelling: A review. Iranian Polymer J. 2010, 19, 375-398.

Wang, D.; Green, MD.; Chen, K.; Daengngam, C.; Kotsuchibashi, Y. Stimuli-responsive polymers: Design, synthesis, characterization, and applications. International Journal of Polymer Science. 2016, 2016. DOI: https://doi.org/10.1155/2016/6480259.

Deepak, K.; Charak, S.; Mehrotra, R.; Kundu, S. FTIR and circular dichroism spectroscopic study of interaction of 5-fluorouracil with DNA. Journal of Photochemistry and Photobiology B: Biology. 2011, 105, 143–148. DOI: https://doi.org/10.1016/j.jphotobiol.2011.08.003.

http://www.cancerresearchuk.org/about-cancer/cancer-in-general/treatment/cancer-drugs/drugs/fluorouracil (Accessed, October 27th 2017).

Olukman, M.; Şanl, O.; Kondolot-Solak, E. Release of anticancer drug 5-Fluorouracil from different ionically crosslinked alginate beads. Journal of Biomaterials and Nanobiotechnology. 2012, 3, 469-479. DOI: https://doi.org/10.4236/jbnb.2012.34048.

Zhang, N.; Yin, Y.; Xu, S. J.; Chen, W. S. 5-Fluorouracil: Mechanisms of resistance and reversal strategies. Molecules. 2008, 13, 1551-1569. DOI: https://doi.org/10.3390/molecules13081551

Kumar, B. A. Imiquimod - Its role in the treatment of cutaneous malignancies.Indian J Pharmacol. 2015, 47, 354–359. DOI: https://doi.org/10.4103/0253-7613.161249

Pharmaceutical Benefits Branch. Aldara public summary document. PBAC meeting July 2006. http://www.health.gov.au/internet/wcms/publishing.nsf/Content/pbac-psd-imiquimod-july06 (Accessed, August 7th 2017).

Sauder, D. N. Imiquimod: Modes of action. British Journal of Dermatology. 2003, 149, 5–8. DOI:https://doi.org/10.1046/j.0366-077x.2003.05628.x

Schön, M.P; Schön, M. Imiquimod: Mode of action. British Journal of Dermatology. 2007, 157, 8–13. DOI: https://doi.org/10.1111/j.1365-2133.2007.08265.x

Martí, M. A. Simulación computacional de biomoléculas. un punto de encuentro entre la físico-química y la biología computacional. Anales Acad. Nac. de Cs. Ex., Fís. y Nat. 2013, 65, 43-49.

Favila-Pérez, MA. Actividad química teórica de fármacos contra mycobacterium tuberculosis favorecida por nanotubos y fullerenos. Ph.D. CIMAV, https://cimav.repositorioinstitucional.mx/jspui/bitstream/1004/223/1/Tesis%20Mar%C3%ADa%20Alejandra%20F%C3%A1vila%20P%C3%A9rez.pdf (Accessed, august 10th 2017).

Ferreira, LG.; Dos-Santos, R. N.; Oliva, G.; Andricopulo, A. D. Molecular docking and structure-based drug design strategies. Molecules. 2015, 20, 13384-13421. DOI: https://doi.org/10.3390/molecules200713384.

Stewart, J. J. P. Optimization of parameters for semi empirical methods IV: Extension of MNDO, AM1, and PM3 to more main group elements. J. Mol. Model.2004, 10, 155–164. DOI: https://doi.org/10.1007/s00894-004-0183-z.

Mendieta-Moreno, J. I.; Walker, R.; Lewis, J. P.; Gomez-Puertas, P.; Mendieta, J.; Ortega, J. FIREBALL/AMBER: An efficient local-orbital DFT QM/MM method for biomolecular systems. J. Chem. Theory Comput.2014, 10, 2185–2193. DOI: https://doi.org/10.1021/ct500033w.

Suarez, C.; Simulación con dinámica molecular de polímeros anfifílicos: dependencia del ph, longitud de la cadena polimérica y cadena alquílica. B.Sc. Universidad ICESI, 2013. https://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/76492/1/simulacion_dinamica_molecular.pdf (Accessed, August 10th 2017).

Young, DC. (eds). Computational chemistry: A practical guide for applying techniques to real-world problems. WILEY, 2001. ISBN: 0-471-22065-5.

Parmar, NS.; Jethara, SI.; Patel, AD.; Patel, MR. A review literature and optimization of controlled drug delivery system using artificial neural network. JPSBR. 2015, 5, 306-314.

Mendyk, A.; Jachowicz, R.; Dorozynski, P. Artificial neural networks in the modeling of drugs release profiles from hydro dynamically balanced systems. Acta Poloniae Pharmaceutica Drug Research.2006, 63, 75-80. DOI: https://doi.org/10.1155/2015/863874.

http://chemistry.oregonstate.edu/courses/ch361-464/ch463/HYPERCH98.htm (Accessed, august 7th 2017).

Belaidi, S.; Mellaoui, M.; Electronic structure and physical-chemistry property relationship for oxazole derivatives by AB initio and DFT methods. Org. Chem. Int. 2011, 2011, 1-7.DOI: https://doi.org/10.1155/2011/254064.

Almi, Z., Belaidi, S.; Lanez, T.; Tchouar, N. Structure activity relationships, qsar modeling and drug-like calculations of tp inhibition of 1,3,4- oxadiazoline-2-thione derivatives. Int. Lett. Chem., Phys. Astron. 2014, 37, 113-124. DOI: https://doi.org/10.18052/www.scipress.com/ILCPA.37.113.

Bakkialakshmi, S.; Chandrakala, D. Thermodynamic studies on the interaction of 5-Fluorouracil with human serum albumin. Int. J. Pharm. Pharm. Sci. 2012, 5, 46-49. DOI: https://doi.org/10.1248/cpb.28.535.

Chao, K. P.; Lu, Y. T.; Yang, H. W. Prediction of partition coefficients of organic compounds between SPME/PDMS and aqueous solution. Int. J. Mol. Sci. 2014, 15, 2585–2595. DOI: https://doi.org/10.1016/j.aca.2015.09.010.

Yassin, A. E. B. ; Anwer, K.; Mowafy, H. A.; El-Bagory, I. M.; Bayomi, M. A.; Alsarra, I. A. Optimization of 5-fluorouracil solid-lipid nanoparticles: a preliminary study to treat colon cancer. Int. J. Med. Sci. 2010, 7, 398-408. DOI: https://doi.org/10.7150/ijms.7.398.

Bilensoy, E.; Curpanli, Y.; Sen, M.; Dogan, L.; Cahs, S. Thermosensitive muco adhesive gel formulation loaded with 5-Fu: cyclodextrin complex for HPV-induced cervical cancer. J. Incl. Phenom. Macrocycl. Chem. 2007, 57, 363-370. DOI: https://doi.org/10.1007/s10847-006-9259-y.

Garea, S. A.; Ghebaur, A.; Andronescu, C. Systems Based on Dendrimers and Antitumoral Drug Synthesized by Non-covalent Method the influence of dendrimers generation. Materiale Plastice. 2011, 48, 17-22.

Sunkara, S.; Sravanthi, D.; Maheswari, KM.; Salma, S.; Nallur, B. N. Development of modified release tablet dosage forms of capecitabine for better therapeutic efficacy. J. Chem. Pharm. Res. 2013, 5, 320-328.

Olukman, M.; Şanli, O.; Kondolot, E. Release of Anticancer Drug 5-Fluorouracil from Different Ionically Crosslinked Alginate Beads. J. Biomater. Nanobiotechnol. 2012, 3, 469-479. DOI: https://doi.org/10.4236/jbnb.2012.34048.

Dinesha.; Viveka, S.; Sandeep S. Laxmeshwar and GundibasappaKarikannarNagaraja. 1-{4-[(1-Isobutyl-1H-imidazo[4,5-c]quinolin- 4yl)amino]phenyl}ethanone. Molbank. 2012, M788; DOI: https://doi.org/10.3390/M788.

Klein, M. P.; Hackenhaar, C. R.; Lorenzoni, S. G.; Rodrigues, R. C.; Costa, T. M. H.; Ninow, J. L.; Hertz, P. F. Chitosan crosslinked with genipin as support matrix for application infood process: Support characterization and β-D-galactosidase immobilization. CarbohydratePolymers. 2016, 137, 184–190.https://doi.org/10.1016/j.carbpol.2015.10.069.

Dimida, S.; Barca, A.; Cancelli, N.; Grazia, R. M.; Demitri, C. Effects of Genipin Concentration on Cross-Linked Chitosan Scaffolds for Bone Tissue Engineering: Structural Characterization and Evidence of Biocompatibility Features. Int. J. Polym. Sci. 2017. DOI:https://doi.org/10.1155/2017/8410750.

Mirzaeil, E.; Faridi-Majidi, R.; Shokrgozar, M. A.; Asghari, P. F. Genipin cross-linked electrospun chitosan-based nanofibrous mat as tissue engineering scaffold. Nanomedicine J. 2014, 1, 137-146.

Rangel-Vázquez, N. A.; Rodríguez-Felix, F. Computational Chemistry Applied in the Analyses of Chitosan/Polyvinylpyrrolidone/Mimosa Tenuiflore (1st Ed.), 2013, Science Publishing Group Ed. Hong Kong.

Hamedani, S. Structural and electronic properties of folic acid adsorption on the carbon nanotubes: A density functional theory study. Orient. J. Chem. 2015, 31, 345-351. DOI:http://dx.doi.org/10.13005/ojc/310140

Stipdonk, M. J.; Badia-Martinez, D.; Sluijter, M.; Offringa, R.; Hall, T. V.; Achour, A. Design of agonistic altered peptides for the robust induction of ctl directed towards h-2db in complex with the melanoma-associated epitope gp100. Cancer Res. 2009, 69, 7784-7792. DOI: https://doi.org/10.1158/0008-5472.

Escobar, J. L.; García, D. M.; Zaldivar. D.: Katime, I. Hidrogeles. principales características en el diseño de sistemas de liberación controlada de fármacos. Rev. Iberoamer. Polím. 2002, 3, 1-25.

Rizwan, M.; Yahya, R.; Hassan, A.; Yar, M.; Azzahari, A. D.; Selvanathan, V.; Sonsudin, F.; Abouloula, C. N. pH sensitive hydrogels in drug delivery: Brief history, properties, swelling, and release mechanism, material selection and applications. Polymers. 2017, 9, 137; DOI: https://doi.org/10.3390/polym9040137.

Kirsch, P. Modern fluoroorganic chemistry: synthesis, reactivity, applications. Wiley-VCH, 2004.

http://www.ifsc.usp.br/~lavfis2/BancoApostilasImagens/ApLuminescencia/Infrared%20Spectroscop1.pdf (Accessed, August 13th 2017).

Farquharson, S.; Gift, A.; Shende, C.; Inscore, F.; Ordway, B.; Farquharson, C.; Murren, J. Surface-enhanced Raman spectral measurements of 5-Fluorouracil in saliva. Molecules. 2008, 13, 2608-2627. DOI: https://doi.org/10.3390/molecules13102608.

Pasqui, D.; Cagna, M.; Barbucci, R. Polysaccharide-Based Hydrogels: The key role of water in affecting mechanical properties. Polymers. 2012, 4, 1517-1534; DOI:https://doi.org/10.3390/polym4031517.

Kurecic, M.; Sfiligoj-Smole, M.; Stana-Kleinschek, K. UV polymerization of poly (n-isopropylacrylamide) hydrogel. Materials and technology. 2012, 46, 87–91.

Mata, I.; Espinosa, E.; Molins, E. Zero-flux surfaces of the electrostatic potential: The border of influence zones of nucleophilic and electrophilic sites in crystalline environment. J. Phys. Chem. A, 2007, 111, 9859–9870. DOI: https://doi.org/10.1021/jp074032l.

Kim, D.; Wang, L. et al. (2R)-4-Oxo-4-[3-(Trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin- 7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine: A Potent, Orally Active Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes. J. Med. Chem., 2005, 48, 141–151. DOI: https://doi.org/10.1021/jm0493156.

http://adsabs.harvard.edu/abs/2015ApSS.359.474S (Accessed, august 13th 2017).

Fraser-Steele, D.; Moreton, R. C.; Staniforth, J. N.; Young, P. M.; Tobyn, M. J.; Edge, S. Surface Energy of Microcrystalline Cellulose Determined by Capillary Intrusion and Inverse Gas Chromatography. AAPS J. 2008, 10, 494–503. DOI: https://doi.org/10.1208/s12248-008-9057-0.

Zhang, R.; Somasundaran, P. Advances in adsorption of surfactants and their mixtures at solid/solution interfaces. Adv. Colloid Interface Sci. 2006, 123–126, 213–229. DOI: https://doi.org/10.1016/j.cis.2006.07.004.

Dimensions

PlumX

Visitas a la página del resumen del artículo

1574

Descargas

Los datos de descarga aún no están disponibles.

Cómo citar

[1]
N. A. Rangel-Vázquez, D. N. Villanueva-García, y J. Kalla, «Análisis estructural de los procesos de adsorción de 5FU e imiquimod en hidrogeles utilizando el modelo híbrido AMBER/PM3», Rev. Colomb. Quim., vol. 47, n.º 2, pp. 28–35, may 2018, doi: 10.15446/rev.colomb.quim.v47n2.67352.