Self-assembling surfactant-like peptide A6K as potential delivery system for hydrophobic drugs

International Journal of Nanomedicine

Volumn 10, Issue , 2015, Pages 847-858

  Chen, Yongzhu ^a   Tang, Chengkang ^b   Zhang, Jie ^b   Gong, Meng ^b   Su, Bo ^b   Qiu, Feng ^b  

^a SICHUAN UNIVERSITY   (China)

^b SICHUAN UNIVERSITY   (China)

Author keywords

Drug delivery; Micelles; Nanofibers; Pyrene; Self assembling peptide

Indexed keywords

ALANYLALANYLALANYLALANYLALANYLALANYLLYSINE; MONOMER; NANOFIBER; PEPTIDE; PYRENE; UNCLASSIFIED DRUG; ACETYL-ALANYL-ALANYL-ALANYL-ALANYL-ALANYL-ALANYL-LYSINE; DRUG CARRIER; LUNG SURFACTANT; NANOMATERIAL; OLIGOPEPTIDE; PYRENE DERIVATIVE; SURFACTANT;

ARTICLE; CONTROLLED STUDY; CRYSTALLIZATION; DRUG DELIVERY SYSTEM; HUMAN; HUMAN CELL; HYDROPHOBICITY; LIVER CELL; MICELLE; MOLECULAR STABILITY; NANOENCAPSULATION; SUSPENSION; ATOMIC FORCE MICROSCOPY; CHEMICAL PHENOMENA; CHEMISTRY; CONFOCAL MICROSCOPY; FLUORESCENCE; HEP-G2 CELL LINE; SPECTROFLUOROMETRY; TRANSMISSION ELECTRON MICROSCOPY;

DRUG CARRIERS; DRUG DELIVERY SYSTEMS; FLUORESCENCE; HEP G2 CELLS; HUMANS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICROSCOPY, ATOMIC FORCE; MICROSCOPY, CONFOCAL; MICROSCOPY, ELECTRON, TRANSMISSION; NANOFIBERS; NANOSTRUCTURES; OLIGOPEPTIDES; PULMONARY SURFACTANTS; PYRENES; SPECTROMETRY, FLUORESCENCE; SURFACE-ACTIVE AGENTS;

EID: 84921951602     PISSN: 11769114     EISSN: 11782013     Source Type: Journal    
DOI: 10.2147/IJN.S71696     Document Type: Article

References (43)

1. Li NN, Lin J, Gao D, Zhang LM. A macromolecular prodrug strategy for combinatorial drug delivery. J Colloid Interface Sci. 2014;417: 301-309.
2. 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;111:825-832.
3. Gu Y, Zhong Y, Meng F, Cheng R, Deng C, Zhong Z. Acetal- linked paclitaxel prodrug micellar nanoparticles as a versatile and potent platform for cancer therapy. Biomacromolecules. 2013;14: 2772-2780.
4. Yu P, Xia XM, Wu M, et al. Folic acid-conjugated iron oxide porous nanorods loaded with doxorubicin for targeted drug delivery. Colloids Surf B Biointerfaces. 2014;120:142-151.
5. Li Q, Lv S, Tang Z, et al. A codelivery system based on paclitaxel grafted mPEG-b-PLG loaded with doxorubicin: preparation, in vitro and in vivo evaluation. Int J Pharm. 2014;471:412-420.
6. Hira SK, Mishra AK, Ray B, Manna PP. Targeted delivery of doxorubicin-loaded poly (epsilon-caprolactone)-b-poly (N-vinylpyrrolidone) micelles enhances antitumor effect in lymphoma. PLoS One. 2014;9:e94309.
7. Chen J, Lu WL, Gu W, et al. Drug-in-cyclodextrin-in-liposomes: a promising delivery system for hydrophobic drugs. Expert Opin Drug Deliv. 2014;11:565-577.
8. Li F, Zhu A, Song X, Ji L. Novel surfactant for preparation of poly(L- lactic acid) nanoparticles with controllable release profile and cytocompatibility for drug delivery. Colloids Surf B Biointerfaces. 2014; 115:377-383.
9. Byagari K, Shanavas A, Rengan AK, Kundu GC, Srivastava R. Biocompatible amphiphilic pentablock copolymeric nanoparticles for anticancer drug delivery. J Biomed Nanotechnol. 2014;10: 109-119.
10. Battogtokh G, Ko YT. Self-assembled polymeric nanoparticle of PEGylated chitosanceramide conjugate for systemic delivery of paclitaxel. J Drug Target. 2014;22:813-821.
11. Perez E, Fernandez A, Olmo R, Teijon JM, Blanco MD. pH and glutathion-responsive hydrogel for localized delivery of paclitaxel.Colloids Surf B Biointerfaces. 2014;116:247-256.
12. Cho JK, Kuh HJ, Song SC. Injectable poly(organophosphazene) hydrogel system for effective paclitaxel and doxorubicin combination therapy. J Drug Target. 2014;22:761-777.
13. Tsai HC, Lin JY, Maryani F, Huang CC, Imae T. Drugloading capacity and nuclear targeting of multiwalled carbon nanotubes grafted with anionic amphiphilic copolymers. Int J Nanomedicine. 2013; 8:4427-4440.
14. Arya N, Arora A, Vasu KS, Sood AK, Katti DS. Combination of single walled carbon nanotubes/graphene oxide with paclitaxel: a reactive oxygen species mediated synergism for treatment of lung cancer. Nanoscale. 2013;5:2818-2829.
15. Gu YJ, Cheng J, Jin J, Cheng SH, Wong WT. Developmentandevaluation of pH-responsive single-walledcarbon nanotube-doxorubicin complexes in cancer cells. Int J Nanomedicine. 2011;6:2889-2898.
16. Bertrand N, Wu J, Xu X, Kamaly N, Farokhzad OC. Cancer nanotechnology: the impact of passive and active targeting in the era of modern cancer biology. Adv Drug Deliv Rev. 2014;66:2-25.
17. Dawidczyk CM, Kim C, Park JH, et al. State-of-the-art in design rules for drug delivery platforms: lessons learned from FDA-approved nanomedicines. J Control Release. 2014;187:133-144.
18. Lakshmanan A, Zhang S, Hauser CA. Short self-assembling peptides as building blocks for modern nanodevices. Trends Biotechnol. 2012;30:155-165.
19. Liu J, Zhao X. Design of selfassembling peptides and their biomedical applications. Nanomedicine (Lond). 2011;6:1621-1643.
20. Lv S, Tang Z, Li M, et al. Co-delivery of doxorubicin and paclitaxelby PEG-polypeptide nanovehicle for the treatment of non-small cell lung cancer. Biomaterials. 2014;35:6118-6129.
21. Liu J, Xu H, Zhang Y, et al. Novel tumor-targeting, self-assembling peptide nanofiber as a carrier for effective curcumin delivery. Int J Nanomedicine. 2014;9:197-207.
22. Zhang P, Cheetham AG, Lin YA, Cui H. Self-assembled Tat nanofibers as effective drug carrier and transporter. ACS Nano. 2013;7:5965-5977.
23. Sadatmousavi P, Mamo T, Chen P. Diethylene glycol functionalized self-assembling peptide nanofibers and their hydrophobic drug delivery potential. Acta Biomater. 2012;8:3241-3250.
24. Soukasene S, Toft DJ, Moyer TJ, et al. Antitumor activity of peptide amphiphile nanofiber-encapsulated camptothecin. ACS Nano. 2011;5:9113-9121.
25. Liu J, Zhang L, Yang Z, Zhao X. Controlled release of paclitaxel from a self-assembling peptide hydrogel formed in situ and antitumor study in vitro. Int J Nanomedicine. 2011;6:2143-2153.
26. Keyes-Baig C, Duhamel J, Fung SY, Bezaire J, Chen P. Self-assembling peptide as a potential carrier of hydrophobic compounds. J Am Chem Soc. 2004;126:7522-7532.
27. Li SD, Huang L. Pharmacokinetics and biodistribution of nanoparticles. Mol Pharm. 2008;5:496-504.
28. Geng Y, Dalhaimer P, Cai S, et al. Shape effects of filaments versus spherical particles in flow and drug delivery. Nat Nanotechnol. 2007; 2:249-255.
29. Lim YB, Lee E, Lee M. Controlled bioactive nanostructures from self-assembly of peptide building blocks. Angew Chem Int Ed. 2007;46:9011-9014.
30. Zhang S. Lipid-like self-assembling peptides. Acc Chem Res. 2012;45: 2142-2150.
31. Zhao X. Design of self-assembling surfactant-like peptides and their applications. Curr Opin Colloid Interface Sci. 2009;14:340-348.
32. Vauthey S, Santoso S, Gong H, Watson N, Zhang S. Molecular selfassembly of surfactant-like peptides to form nanotubes and nanove- sicles. Proc Natl Acad Sci U S A. 2002;99:5355-5360.
33. Maltzahn G, Vauthey S, Santoso S, Zhang S. Positively charged surfactant-like peptides self-assemble into nanostructures. Langmuir. 2003;19:4332-4337.
34. Ge B, Yang F, Yu D, Liu S, Xu H. Designer amphiphilic short pep- tides enhance thermal stability of isolated photosystemI. PLoS One. 2010;5:e10233.
35. Matsumoto K, Vaughn M, Bruce BD, Koutsopoulos S, Zhang S. Designer peptide surfactants stabilize functional photosystem-I membrane complex in aqueous solution for extended time. J Phys Chem B. 2009;113:75-83.
36. Zhao X, Nagai Y, Reeves PJ, Kiley P, Khorana HG, Zhang S. Designer short peptide surfactants stabilize G protein-coupled receptor bovine rhodopsin. Proc Natl Acad Sci U S A. 2006;103:17707-17712.
37. Qiu F, Chen Y, Zhao X. Comparative studies on the self-assembling behaviors of cationic and catanionic surfactant-like peptides. J Colloid Interface Sci. 2009;336:477-484.
38. Zhang H, Li Z, Xu P, Wu R, Jiao Z. A facile two step synthesis of novel chrysanthemum-like mesoporous silica nanoparticles for controlled pyrene release. Chem Commun (Camb). 2010;46:6783-6785.
39. Schatz C, Smith EG, Armes SP, Wanless EJ. Reversible pH-triggered encapsulation and release of pyrene by adsorbed block copolymer micelles. Langmuir. 2008;24:8325-8331.
40. Manna U, Patil S. Encapsulation of uncharged water-insoluble organic substance in polymeric membrane capsules via layer-by-layer approach.J Phys Chem B. 2008;112:13258-13262.
41. Li F, Wang J, Tang F, et al. Fluorescence studies on a designed selfassembling peptide of RAD16-II as a potential carrier for hydrophobic drug. J Nanosci Nanotechnol. 2009;9:1611-1614.
42. Tang F, Zhao X. Interaction between a self-assembling peptide and hydrophobic compounds. J Biomater Sci Polym Ed. 2010;21:677-690.
43. Yekta A, Xu B, Duhamel J, Adiwidjaja H, Winnik MA. Fluorescence studies of associating polymers in water: determination of the chain end aggregation number and a model for the association process. Macromolecules. 1995;28:956-966.