journal article·2014-12

Self-assembled nanocomplexes of anionic pullulan and polyallylamine for DNA and pH-sensitive intracellular drug delivery

Lalit Vora, Monica Tyagi, Ketan Patel, Sanjay Gupta, Pradeep Vavia

Journal of Nanoparticle Research· Volume 16· Issue 12
Publisher page

Abstract

The amalgamation of chemotherapy and gene therapy is promising treatment option for cancer. In this study, novel biocompatible self-assembled nanocomplexes (NCs) between carboxylmethylated pullulan t335 (CMP) with polyallylamine (CMP–PAA NCs) were developed for plasmid DNA (pDNA) and pH-sensitive doxorubicin (DOX) delivery. DOX was conjugated to CMP (DOX–CMP) via hydrazone and confirmed by FTIR and 1H-NMR. In vitro release studies of pH-sensitive DOX–CMP conjugate showed 23 and 85 % release after 48 h at pH 7.4 (physiological pH) and pH 5 (intracellular/tumoral pH), respectively. The CMP–PAA NCs or DOX–CMP–PAA NCs self-assembled into a nanosized (<250 nm) spherical shape as confirmed by DLS and TEM. The hemolysis and cytotoxicity study indicated that the CMP–PAA NCs did not show cytotoxicity in comparison with plain polyallylamine. Gel retardation assay showed complete binding of pDNA with CMP–PAA NCs at 1:2 weight ratio. CMP–PAA NCs/pDNA showed significantly higher transfection in HEK293 cells compared to PAA/pDNA complexes. Confocal imaging demonstrated successful cellular uptake of DOX–CMP–PAA NCs in HEK293 cells. Thus, NCs hold great potential for targeted pDNA and pH-sensitive intratumoral drug delivery.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: RNA Interference and Gene Delivery · Nanoparticle-Based Drug Delivery · Dendrimers and Hyperbranched Polymers

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (39)

Show source-provided references
1. Boussif O, Delair T, Brua C, Veron L, Pavirani A, Kolbe HV (1999) Synthesis of polyallylamine derivatives and their use as gene transfer vectors in vitro. Bioconjugate Chem 10:877–88310.1021/bc9900439 ↗
2. Chang RS, Suh MS, Kim S, Shim G, Lee S, Han SS, Oh YK (2011) Cationic drug-derived nanoparticles for multifunctional delivery of anticancer siRNA. Biomaterials 32:9785–979510.1016/j.biomaterials.2011.09.017 ↗
3. Chen C, Jones HC, Mistriotis P, Yua Y, Maa X, Ravikrishnan A, Jiang M, Andreadis TS, Blaine AP, Cheng C (2013) Poly(ethylene glycol)-block-cationic polylactide nanocomplexes of differing charge density for gene delivery. Biomaterials 34:9688–969910.1016/j.biomaterials.2013.08.063 ↗
4. Dulong V, Mocanu G, Picton L, Cerf DL (2012) Amphiphilic and thermosensitive copolymers based on pullulan and Jeffamine®: synthesis, characterization and physicochemical properties. Carbohyd Polym 87:1522–153110.1016/j.carbpol.2011.09.049 ↗
5. Eldar-boock A, Polyak D, Scomparin A, Satchi-fainaro R (2013) Nano-sized polymers and liposomes designed to deliver combination therapy for cancer. Curr Opin Biotech 24:682–68910.1016/j.copbio.2013.04.014 ↗
6. Faizuloev E, Marova A, Nikonova A, Volkova I, Gorshkova M, Izumrudovc V (2012) Water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl]chitosan chloride as a nucleic acids vector for cell transfection. Carbohyd Polym 89:1088–109410.1016/j.carbpol.2012.03.071 ↗
7. Fan J, Zeng F, Xu J, Wu S (2013) Targeted anti-cancer prodrug based on carbon nanotube with photodynamic therapeutic effect and pH-triggered drug release. J Nanopart Res 15:191110.1007/s11051-013-1911-z ↗
8. Guo H, Lai Q, Wang W, Wu Y, Zhang C, Liu Y, Yuan Z (2013) Functional alginate nanoparticles for efficient intracellular release of doxorubicin and hepatoma carcinoma cell targeting therapy. Int J Pharm 451:1–1110.1016/j.ijpharm.2013.04.025 ↗
9. Haratake M, Matsumoto S, Ono M, Nakayama M (2008) Nanoparticulate glutathione peroxidase mimics based on selenocystine—pullulan conjugates. Bioconjugate Chem 19:1831–183910.1021/bc800086z ↗
10. Hosseinkhani H, He W, Chiang C, Hong P, Yu D, Domb AJ, Ou K (2013) Biodegradable nanoparticles for gene therapy technology. J Nanopart Res 15:179410.1007/s11051-013-1794-z ↗
11. Hou L, Fan Y, Yao J, Zhou J, Li C, Fang Z, Zhang Q (2011) Low molecular weight heparin-all-trans-retinoid acid conjugate as a drug carrier for combination cancer chemotherapy of paclitaxel and all-trans-retinoid acid. Carbohydrate Polym 86:1157–116610.1016/j.carbpol.2011.06.008 ↗
12. Jiang T, Li Y, Lv Y, Cheng Y, He F, Zhuo R (2013) Amphiphilic polycarbonate conjugates of doxorubicin with pH-sensitive hydrazone linker for controlled release. Colloid Surf B 111:542–54810.1016/j.colsurfb.2013.06.054 ↗
13. Li F, Zhang H, Gu C, Fan L, Qiao Y, Tao Y, Yi J (2013a) Self-assembled nanoparticles from folate-decorated maleilated pullulan-doxorubicin conjugate for improved drug delivery to cancer cells. Polym Int 62:165–17110.1002/pi.4272 ↗
14. Li H, Bian S, Huang Y, Liang J, Fan Y, Zhang X (2013b) High drug loading pH-sensitive pullulan-DOX conjugate nanoparticles for hepatic targeting. J Biomed Mater Res 102:150–15910.1002/jbm.a.34680 ↗
15. Lu D, Wen X, Liang J, Gu Z, Zhang X, Fan Y (2009) A pH-sensitive nano drug delivery system derived from pullulan/doxorubicin conjugate. J Biomed Mater Res 89:177–18310.1002/jbm.b.31203 ↗
16. Masereel B, Dinguizli M, Bouzin C, Moniotte N, Feron O, Gallez B, Borght TV, Michiels C, Lucas S (2011) Antibody immobilization on gold nanoparticles coated layer-by-layer with polyelectrolytes. J Nanopart Res 13:1573–158010.1007/s11051-010-9908-3 ↗
17. Misra R, Acharya S, Sahoo SK (2010) Cancer nanotechnology: application of nanotechnology in cancer therapy. Drug Discov Today 15:842–85010.1016/j.drudis.2010.08.006 ↗
18. Mocanu G, Nichifor M, Picton L, About-Jaudet E, Cerf DL (2014) Preparation and characterization of anionic pullulan thermoassociative nanoparticles for drug delivery. Carbohyd Polym 111:892–90010.1016/j.carbpol.2014.05.037 ↗
19. Nimesh S, Kumar R, Chandra R (2006) Novel polyallylamine—dextran sulfate – DNA nanoplexes : highly efficient non-viral vector for gene delivery. Int J Pharm 320(14):3–149
20. Ogris M, Brunner S, Schüller S, Kircheis R, Wagner E (1999) PEGylated DNA/transferrin-PEI complexes: reduced interaction with blood components, extended circulation in blood and potential for systemic gene delivery. Gene Ther 6:595–60510.1038/sj.gt.3300900 ↗
21. Parhi P, Mohanty C, Sahoo SK (2012) Nanotechnology-based combinational drug delivery: an emerging approach for cancer therapy. Drug Discov Today 17:1044–105210.1016/j.drudis.2012.05.010 ↗
22. Patel K, Tyagi M, Monpara J, Vora L, Gupta S, Vavia P (2014) Arginoplexes: an arginine-anchored nanoliposomal carrier for gene delivery. J Nanopart Res 16:1–1010.1007/s11051-014-2345-y ↗
23. Pereiraa JM, Mahoney M, Edgar KJ (2014) Synthesis of amphiphilic 6-carboxypullulan ethers. Carbohyd Polym 100:65–7310.1016/j.carbpol.2012.12.029 ↗
24. Petros R, DeSimone JM (2010) Strategies in the design of nanoparticles for therapeutic applications. Nat Rev Drug Discov 9:615–62710.1038/nrd2591 ↗
25. Prajapati VD, Jani GK, Khanda SM (2013) Pullulan: an exopolysaccharide and its various applications. Carbohyd Polym 95:540–54910.1016/j.carbpol.2013.02.082 ↗
26. Priya SS, Rekha MR, Sharma CP (2014) Pullulan—protamine as efficient haemocompatible gene delivery vector: synthesis and in vitro characterization. Carbohyd Polym 102:207–21510.1016/j.carbpol.2013.11.024 ↗
27. Rekha MR, Sharma CP (2011) Hemocompatible pullulan-polyethyleneimine conjugates for liver cell gene delivery: in vitro evaluation of cellular uptake, intracellular trafficking and transfection efficiency. Acta Biomater 7:370–37910.1016/j.actbio.2010.07.027 ↗
28. Samal SK, Dash M, Van Vlierberghe S, Kaplan DL, Chiellini E, van Blitterswijk C, Moronid L, Dubruel P (2012) Cationic polymers and their therapeutic potential. Chem Soc Rev 41:7147–719410.1039/c2cs35094g ↗
29. Sang HY, Lee AE, Park GT (2002) Doxorubicin-conjugated biodegradable polymeric micelles having acid-cleavable linkages. J Control Release 82:17–2710.1016/S0168-3659(02)00088-3 ↗
30. Sarkar K, Kundu PP (2013) PAMAM conjugated chitosan through naphthalimide moiety for enhanced gene transfection efficiency. Carbohyd polym 98:495–50410.1016/j.carbpol.2013.06.006 ↗
31. Scomparin A, Salmaso S, Bersani S, Satchi-Fainaro R, Caliceti P (2011) Novel folated and non-folated pullulan bioconjugates for anticancer drug delivery. Eur J Pharml Sci 42:547–55810.1016/j.ejps.2011.02.012 ↗
32. She W, Luo K, Zhang C, Wang G, Geng Y, Li L, He B, Gu Z (2013) The potential of self-assembled, pH-responsive nanoparticles of mPEGylated peptide d endronedoxorubicin conjugates for cancer therapy. Biomaterials 34:1613–162310.1016/j.biomaterials.2012.11.007 ↗
33. Shuai X, Ai H, Nasongkla N, Kim S, Gao J (2004) Micellar carriers based on block copolymers of poly(epsilon-caprolactone) and poly(ethylene glycol) for doxorubicin delivery. J Control Release 98:415–42610.1016/j.jconrel.2004.06.003 ↗
34. Thakor DK, Teng YD, Tabata Y (2009) Neuronal gene delivery by negatively charged pullulan-spermine/DNA anioplexes. Biomaterials 30:1815–182610.1016/j.biomaterials.2008.12.032 ↗
35. Thomsen LB, Lichota J, Kim KS, Moos T (2011) Gene delivery by pullulan derivatives in brain capillary endothelial cells for protein secretion. J Control Release 151:45–5010.1016/j.jconrel.2011.01.002 ↗
36. Tros de Ilarduya C, Sun Y, Duzgunes N (2010) Gene delivery by lipoplexes and polyplexes. Eur J Pharm Sci 40:159–17010.1016/j.ejps.2010.03.019 ↗
37. Wang C, Luo X, Zhao Y, Han L, Zeng X, Feng M, Wu C (2012) Influence of the polyanion on the physico-chemical properties and biological activities of polyanion/DNA/polycation ternary polyplexes. Acta Biomater 8:3014–302610.1016/j.actbio.2012.04.034 ↗
38. Wang Y, Chen H, Liu Y, Wu J, Zhou P, Wang Y, Zhang N (2013) pH-sensitive pullulan-based nanoparticle carrier of methotrexate and combretastatin A4 for the combination therapy against hepatocellular carcinoma. Biomaterials 34:7181–719010.1016/j.biomaterials.2013.05.081 ↗
39. Xu M, Qian J, Suo A, Wang H, Yong X, Liu X, Liu R (2013) Reduction/pH dual-sensitive PEGylated hyaluronan nanoparticles for targeted doxorubicin delivery. Carbohyd Polym 98:181–18810.1016/j.carbpol.2013.05.077 ↗