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Erschienen in: Journal of Materials Science 16/2017

01.05.2017 | Chemical routes to materials

Amphiphilic polymer–drug conjugates based on acid-sensitive 100% hyperbranched polyacetals for cancer therapy

verfasst von: Xiao Duan, Yalan Wu, Mengsi Ma, Junjie Du, Shan Zhang, Heng Chen, Jie Kong

Erschienen in: Journal of Materials Science | Ausgabe 16/2017

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Abstract

A new type of acid-sensitive 100% hyperbranched polyacetals (HBPA) was synthesized, which could be completely degraded into small molecules under acidic environment and avoid the accumulative toxicity in vivo. The AB2 monomer was synthesized by 4-carboxybenzaldehyde and 2-bromoethanol. The bulk polycondensation was carried out in vacuum environment to remove water byproduct. The massive terminal aldehyde groups of HBPA were conjugated with mPEG-NH2 and doxorubicins to form amphiphilic acid-sensitive polymer–drug conjugates (DOX-HBPA-PEG). The stability of the micelles of DOX-HBPA-PEG was evaluated by DLS at different pH value in phosphate buffer saline (PBS). The DOX release in vitro showed that the cumulative release rate was 14.51% in pH 7.4 PBS after 24 h and the cumulative release rate was 48.56% in pH 6.0 PBS after 24 h. The results of cell viability of DOX-HBPA-PEG and HBPA-PEG showed that the polymer–DOX conjugates were effective drug delivery systems. The uptake process of DOX-HBPA-PEG by A549 cells showed that the micelle was totally swallowed in 1 h later. The controllable drug release nature, stability, biocompatibility and completely degradable structures (acid-sensitive) make them to be promising drug delivery systems.

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Literatur
1.
Zurück zum Zitat Zhang P, Cheng F, Zhou R, Cao J, Li J, Burda C, Min Q, Zhu J (2014) DNA-hybrid-gated multifunctional mesoporous silica nanocarriers for dual-targeted and microRNA-responsive controlled drug delivery. Angew Chem Int Ed 126:2403–2407CrossRef Zhang P, Cheng F, Zhou R, Cao J, Li J, Burda C, Min Q, Zhu J (2014) DNA-hybrid-gated multifunctional mesoporous silica nanocarriers for dual-targeted and microRNA-responsive controlled drug delivery. Angew Chem Int Ed 126:2403–2407CrossRef
2.
Zurück zum Zitat Ma M, Huang Y, Chen H, Jia X, Wang S, Wang Z, Shi J (2015) Bi2S3-embedded mesoporous silica nanoparticles for efficient drug delivery and interstitial radiotherapy sensitization. Biomaterials 37:447–455CrossRef Ma M, Huang Y, Chen H, Jia X, Wang S, Wang Z, Shi J (2015) Bi2S3-embedded mesoporous silica nanoparticles for efficient drug delivery and interstitial radiotherapy sensitization. Biomaterials 37:447–455CrossRef
3.
Zurück zum Zitat Geers B, Dewitte H, De Smedt SC, Lentacker I (2012) Crucial factors and emerging concepts in ultrasound-triggered drug delivery. J Control Release 164:248–255CrossRef Geers B, Dewitte H, De Smedt SC, Lentacker I (2012) Crucial factors and emerging concepts in ultrasound-triggered drug delivery. J Control Release 164:248–255CrossRef
4.
Zurück zum Zitat Soldano C (2015) Hybrid metal-based carbon nanotubes: Novel platform for multifunctional applications. Prog Mater Sci 69:183–212CrossRef Soldano C (2015) Hybrid metal-based carbon nanotubes: Novel platform for multifunctional applications. Prog Mater Sci 69:183–212CrossRef
5.
Zurück zum Zitat Chen P, Hsiao KM, Chou C (2013) Molecular characterization of toxicity mechanism of single-walled carbon nanotubes. Biomaterials 34:5661–5669CrossRef Chen P, Hsiao KM, Chou C (2013) Molecular characterization of toxicity mechanism of single-walled carbon nanotubes. Biomaterials 34:5661–5669CrossRef
6.
Zurück zum Zitat Fan L, Campagnoli S, Wu H, Grandi A, Parri M, Camilli ED, Grandi G, Viale G, PileriP Grifantini R, Song CJ, Jin B (2015) Negatively charged AuNP modified with monoclonal antibody against novel tumor antigen FAT1 for tumor targeting. J Exp Clin Cancer Res 34:103CrossRef Fan L, Campagnoli S, Wu H, Grandi A, Parri M, Camilli ED, Grandi G, Viale G, PileriP Grifantini R, Song CJ, Jin B (2015) Negatively charged AuNP modified with monoclonal antibody against novel tumor antigen FAT1 for tumor targeting. J Exp Clin Cancer Res 34:103CrossRef
7.
Zurück zum Zitat Fan L, Zhang YS, Wang F, Yang Q, Tan J, Grifantini R, Wu H, Song CJ, Jin B (2016) Multifunctional all-in-one drug delivery systems for tumor targeting and sequential release of three different anti-tumor drugs. Biomaterials 76:399–407CrossRef Fan L, Zhang YS, Wang F, Yang Q, Tan J, Grifantini R, Wu H, Song CJ, Jin B (2016) Multifunctional all-in-one drug delivery systems for tumor targeting and sequential release of three different anti-tumor drugs. Biomaterials 76:399–407CrossRef
8.
Zurück zum Zitat Amiri A, Ramazani A, Jahanshahi M, Moghadamnia AA (2016) Synthesis and evaluating of nanoporous molecularly imprinted polymers for extraction of quercetin as a bioactive component of medicinal plants, Iran. J Chem Chem Eng 35(4):11–19 Amiri A, Ramazani A, Jahanshahi M, Moghadamnia AA (2016) Synthesis and evaluating of nanoporous molecularly imprinted polymers for extraction of quercetin as a bioactive component of medicinal plants, Iran. J Chem Chem Eng 35(4):11–19
9.
Zurück zum Zitat Malekzadeh AM, Ramazani A, Rezaei SJT, Niknejad H (2017) Design and construction of multifunctional hyperbranched polymers coated magnetite nanoparticles for both targeting magnetic resonance imaging and cancer therapy. J Colloid Interface Sci 490:64–73CrossRef Malekzadeh AM, Ramazani A, Rezaei SJT, Niknejad H (2017) Design and construction of multifunctional hyperbranched polymers coated magnetite nanoparticles for both targeting magnetic resonance imaging and cancer therapy. J Colloid Interface Sci 490:64–73CrossRef
10.
Zurück zum Zitat Dayyani N, Khoee S, Ramazani A (2015) Design and synthesis of pH-sensitive polyamino-ester magnetodendrimers: surface functional groups effect on viability of human prostate carcinoma cell lines DU145. Eur J Med Chem 98:190–202CrossRef Dayyani N, Khoee S, Ramazani A (2015) Design and synthesis of pH-sensitive polyamino-ester magnetodendrimers: surface functional groups effect on viability of human prostate carcinoma cell lines DU145. Eur J Med Chem 98:190–202CrossRef
11.
Zurück zum Zitat QiaoYB Duan X, Fan L, Li W, Wu H, Wang YK (2014) Synthesis of controlled molecular weight poly (β-malic acid) and conjugation with HCPT as a polymeric drug carrier. J Polym Res 21:397–405CrossRef QiaoYB Duan X, Fan L, Li W, Wu H, Wang YK (2014) Synthesis of controlled molecular weight poly (β-malic acid) and conjugation with HCPT as a polymeric drug carrier. J Polym Res 21:397–405CrossRef
12.
Zurück zum Zitat Li F, Zhang HT, Gu CH, Fan L, QiaoYB Tao YC, Cheng C, Wu H, Yi J (2013) Self-assembled nanoparticles from folate-decorated maleilated pullulan–doxorubicin conjugate for improved drug delivery to cancer cells. Polym Int 62:165–171CrossRef Li F, Zhang HT, Gu CH, Fan L, QiaoYB Tao YC, Cheng C, Wu H, Yi J (2013) Self-assembled nanoparticles from folate-decorated maleilated pullulan–doxorubicin conjugate for improved drug delivery to cancer cells. Polym Int 62:165–171CrossRef
13.
Zurück zum Zitat Li F, Fan L, Li W, Duan X, QiaoYB WuH (2014) Synthesis and micellar characterization of luteinizing hormone-releasing hormone poly(ethylene glycol)- block-poly(l-histidine) copolymers. Polym Eng Sci 55(2):277–286CrossRef Li F, Fan L, Li W, Duan X, QiaoYB WuH (2014) Synthesis and micellar characterization of luteinizing hormone-releasing hormone poly(ethylene glycol)- block-poly(l-histidine) copolymers. Polym Eng Sci 55(2):277–286CrossRef
14.
Zurück zum Zitat Fang J, Nakamura H, Maeda H (2011) The EPR effect: unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect. Adv Drug Deliv Rev 63:136–151CrossRef Fang J, Nakamura H, Maeda H (2011) The EPR effect: unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect. Adv Drug Deliv Rev 63:136–151CrossRef
15.
Zurück zum Zitat Tetsuji Y, Yasuhiko T, Yoshito I (1994) Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice. J Pharm Sci-US 84:601–606 Tetsuji Y, Yasuhiko T, Yoshito I (1994) Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice. J Pharm Sci-US 84:601–606
16.
Zurück zum Zitat Tetsuji Y, Yasuhiko T, Yoshito I (1995) Fate of water-soluble polymers administered via different routes. J Pharm Sci-US 84:349–354CrossRef Tetsuji Y, Yasuhiko T, Yoshito I (1995) Fate of water-soluble polymers administered via different routes. J Pharm Sci-US 84:349–354CrossRef
17.
Zurück zum Zitat Martin EE, Sebastian S, Marc D (2004) Anti-vascular tumor therapy: recent advances, pitfalls and clinical perspectives. Drug Resist Update 7:125–138CrossRef Martin EE, Sebastian S, Marc D (2004) Anti-vascular tumor therapy: recent advances, pitfalls and clinical perspectives. Drug Resist Update 7:125–138CrossRef
18.
Zurück zum Zitat Markovsky E, Baabur-Cohen H, Eldar-Boock A, Omer L, Tiram G, Ferber S, Ofek P, Polyak D, Scomparin A, Satchi-Fainaro R (2012) Administration, distribution, metabolism and elimination of polymer therapeutics. J Control Release 161:446–460CrossRef Markovsky E, Baabur-Cohen H, Eldar-Boock A, Omer L, Tiram G, Ferber S, Ofek P, Polyak D, Scomparin A, Satchi-Fainaro R (2012) Administration, distribution, metabolism and elimination of polymer therapeutics. J Control Release 161:446–460CrossRef
19.
Zurück zum Zitat Hong BJ, Chipre AJ, Nguyen ST (2013) Acid-degradable polymer-caged lipoplex (PCL) platform for siRNA delivery: facile cellular triggered release of siRNA. J Am Chem Soc 135:17655–17658CrossRef Hong BJ, Chipre AJ, Nguyen ST (2013) Acid-degradable polymer-caged lipoplex (PCL) platform for siRNA delivery: facile cellular triggered release of siRNA. J Am Chem Soc 135:17655–17658CrossRef
20.
Zurück zum Zitat Kumar A, Lale SV, Mahajan S, Choudhary V, Koul V (2015) ROP and ATRP fabricated dual targeted redox sensitive polymersomes based on pPEGMA-PCL-ss-PCL-pPEGMA triblock copolymers for breast cancer therapeutics. ACS Appl Mater Interfaces 7:9211–9227CrossRef Kumar A, Lale SV, Mahajan S, Choudhary V, Koul V (2015) ROP and ATRP fabricated dual targeted redox sensitive polymersomes based on pPEGMA-PCL-ss-PCL-pPEGMA triblock copolymers for breast cancer therapeutics. ACS Appl Mater Interfaces 7:9211–9227CrossRef
21.
Zurück zum Zitat Sitia L, Ferrari R, Violatto MB, Talamini L, Dragoni L et al (2016) Fate of PLA and PCL-based polymeric nanocarriers in cellular and animal models of triple-negative breast cancer. Biomacromol 17:744–755CrossRef Sitia L, Ferrari R, Violatto MB, Talamini L, Dragoni L et al (2016) Fate of PLA and PCL-based polymeric nanocarriers in cellular and animal models of triple-negative breast cancer. Biomacromol 17:744–755CrossRef
22.
Zurück zum Zitat Man DKW, Casettari L, Cespi M, Bonacucina G, Palmieri GF et al (2015) Oleanolic acid loaded PEGylated PLA and PLGA nanoparticles with enhanced cytotoxic activity against cancer cells. Mol Pharm 12:2112–2125CrossRef Man DKW, Casettari L, Cespi M, Bonacucina G, Palmieri GF et al (2015) Oleanolic acid loaded PEGylated PLA and PLGA nanoparticles with enhanced cytotoxic activity against cancer cells. Mol Pharm 12:2112–2125CrossRef
23.
Zurück zum Zitat Nascimento AV, Singh A, Bousbaa H, Ferreira D, Sarmento B et al (2015) Combinatorial-designed epidermal growth factor receptor-targeted chitosan nanoparticles for encapsulation and delivery of lipid-modified platinum derivatives in wild-type and resistant non-small-cell lung cancer cells. Mol Pharm 12:4466–4477CrossRef Nascimento AV, Singh A, Bousbaa H, Ferreira D, Sarmento B et al (2015) Combinatorial-designed epidermal growth factor receptor-targeted chitosan nanoparticles for encapsulation and delivery of lipid-modified platinum derivatives in wild-type and resistant non-small-cell lung cancer cells. Mol Pharm 12:4466–4477CrossRef
24.
Zurück zum Zitat Ferreira DP, Conceição DS, Fernandes F, Sousa T, Calhelha RC et al (2016) Characterization of a squaraine/chitosan system for photodynamic therapy of cancer. J Phys Chem B 120:1212–1220CrossRef Ferreira DP, Conceição DS, Fernandes F, Sousa T, Calhelha RC et al (2016) Characterization of a squaraine/chitosan system for photodynamic therapy of cancer. J Phys Chem B 120:1212–1220CrossRef
25.
Zurück zum Zitat Kiani M, MirzazadehTekie FS, Dinarvand M, Soleimani M, Dinarvand R et al (2016) Thiolatedcarboxymethyl dextran as a nanocarrier for colon delivery of hSET1 antisense: in vitro stability and efficiency study. Mater Sci Eng C-Mater 62:771–778CrossRef Kiani M, MirzazadehTekie FS, Dinarvand M, Soleimani M, Dinarvand R et al (2016) Thiolatedcarboxymethyl dextran as a nanocarrier for colon delivery of hSET1 antisense: in vitro stability and efficiency study. Mater Sci Eng C-Mater 62:771–778CrossRef
26.
Zurück zum Zitat Anirudhan TS, Binusreejayan (2016) Dextran based nanosized carrier for the controlled and targeted delivery of curcumin to liver cancer cells. Int J Biol Macromol 88:222–235CrossRef Anirudhan TS, Binusreejayan (2016) Dextran based nanosized carrier for the controlled and targeted delivery of curcumin to liver cancer cells. Int J Biol Macromol 88:222–235CrossRef
27.
Zurück zum Zitat Tarvirdipour S, Vasheghani-Farahani E, Soleimani M, Bardania H (2016) Functionalized magnetic dextran-spermine nanocarriers for targeted delivery of doxorubicin to breast cancer cells. Int J Pharm 501:331–341CrossRef Tarvirdipour S, Vasheghani-Farahani E, Soleimani M, Bardania H (2016) Functionalized magnetic dextran-spermine nanocarriers for targeted delivery of doxorubicin to breast cancer cells. Int J Pharm 501:331–341CrossRef
28.
Zurück zum Zitat Tomalova B, Sirova M, Rossmann P, Pola R, Strohalm J et al (2016) The structure-dependent toxicity, pharmacokinetics and anti-tumour activity of HPMA copolymer conjugates in the treatment of solid tumours and leukaemia. J Control Release 223:1–10CrossRef Tomalova B, Sirova M, Rossmann P, Pola R, Strohalm J et al (2016) The structure-dependent toxicity, pharmacokinetics and anti-tumour activity of HPMA copolymer conjugates in the treatment of solid tumours and leukaemia. J Control Release 223:1–10CrossRef
29.
Zurück zum Zitat Mao J, Li Y, Wu T, Yuan C, Zeng B et al (2016) A simple dual-pH responsive prodrug-based polymeric micelles for drug delivery. ACS Appl Mater Interfaces 8:17109–17117CrossRef Mao J, Li Y, Wu T, Yuan C, Zeng B et al (2016) A simple dual-pH responsive prodrug-based polymeric micelles for drug delivery. ACS Appl Mater Interfaces 8:17109–17117CrossRef
30.
Zurück zum Zitat Zhang Y, Xiao C, Ding J, Li M, Chen X et al (2016) A comparative study of linear, Y-shaped and linear-dendritic methoxy poly(ethylene glycol)-block-polyamidoamine-block-poly(l-glutamic acid) block copolymers for doxorubicin delivery in vitro and in vivo. Acta Biomater 40:243–253CrossRef Zhang Y, Xiao C, Ding J, Li M, Chen X et al (2016) A comparative study of linear, Y-shaped and linear-dendritic methoxy poly(ethylene glycol)-block-polyamidoamine-block-poly(l-glutamic acid) block copolymers for doxorubicin delivery in vitro and in vivo. Acta Biomater 40:243–253CrossRef
31.
Zurück zum Zitat Chen P, Qiu M, Deng C, Meng F, Zhang J et al (2015) pH-responsive chimaericpepsomes based on asymmetric poly(ethyleneglycol)-b-poly(l-leucine)-b-poly(l-glutamic acid) triblock copolymer for efficient loading and active intracellular delivery of doxorubicin hydrochloride. Biomacromolecules 16:1322–1330CrossRef Chen P, Qiu M, Deng C, Meng F, Zhang J et al (2015) pH-responsive chimaericpepsomes based on asymmetric poly(ethyleneglycol)-b-poly(l-leucine)-b-poly(l-glutamic acid) triblock copolymer for efficient loading and active intracellular delivery of doxorubicin hydrochloride. Biomacromolecules 16:1322–1330CrossRef
32.
Zurück zum Zitat Chen FM, Lu H, Wu LA, Gao LN, An Y et al (2013) Surface-engineering of glycidylmethacrylated dextran/gelatin microcapsules with thermo-responsive poly(N-isopropylacrylamide) gates for controlled delivery of stromal cell-derived factor-1α. Biomaterials 34:6515–6527CrossRef Chen FM, Lu H, Wu LA, Gao LN, An Y et al (2013) Surface-engineering of glycidylmethacrylated dextran/gelatin microcapsules with thermo-responsive poly(N-isopropylacrylamide) gates for controlled delivery of stromal cell-derived factor-1α. Biomaterials 34:6515–6527CrossRef
33.
Zurück zum Zitat Li F, Wu H, Fan L, Zhang HT, Zhang H, Gu CH (2009) Study of dual responsive poly[(maleilated dextran)-graft-(N-isopropylacrylamide)] hydrogel nanoparticles: preparation, characterization and biological evaluation. Polym Int 58:1023–1033CrossRef Li F, Wu H, Fan L, Zhang HT, Zhang H, Gu CH (2009) Study of dual responsive poly[(maleilated dextran)-graft-(N-isopropylacrylamide)] hydrogel nanoparticles: preparation, characterization and biological evaluation. Polym Int 58:1023–1033CrossRef
34.
Zurück zum Zitat Fan L, Li F, Zhang HT, Wang YK, Cheng C, Li XY, Gu CH, Yang Q, Wu H, Zhang SY (2010) Co-delivery of PDTC and doxorubicin by multifunctional micellar nanoparticles. Biomaterials 31:5634–5642CrossRef Fan L, Li F, Zhang HT, Wang YK, Cheng C, Li XY, Gu CH, Yang Q, Wu H, Zhang SY (2010) Co-delivery of PDTC and doxorubicin by multifunctional micellar nanoparticles. Biomaterials 31:5634–5642CrossRef
35.
Zurück zum Zitat Wu H, Zhu L, Torchilin VP (2013) pH-sensitive poly(histidine)-PEG/DSPE-PEG co-polymer micelles for cytosolic drug delivery to achieve active targeted drug delivery and overcome multidrug resistance. Biomaterials 34:1213–1222CrossRef Wu H, Zhu L, Torchilin VP (2013) pH-sensitive poly(histidine)-PEG/DSPE-PEG co-polymer micelles for cytosolic drug delivery to achieve active targeted drug delivery and overcome multidrug resistance. Biomaterials 34:1213–1222CrossRef
36.
Zurück zum Zitat Li DD, Wang JX, Ma Y, Qian HS, Wang D, Wang L, Zhang GB, QiuLZ Wang YC, Yang XZ (2016) A donor–acceptor conjugated polymer with alternating isoindigo derivative and bithiophene units for near-infrared modulated cancer thermo-chemotherapy. ACS Appl Mater Interfaces 8:19312–19320CrossRef Li DD, Wang JX, Ma Y, Qian HS, Wang D, Wang L, Zhang GB, QiuLZ Wang YC, Yang XZ (2016) A donor–acceptor conjugated polymer with alternating isoindigo derivative and bithiophene units for near-infrared modulated cancer thermo-chemotherapy. ACS Appl Mater Interfaces 8:19312–19320CrossRef
37.
Zurück zum Zitat Wang JX, Liu Y, Ma YC, Sun CY, Tao W, Wang YC, Yang XZ, Wang J (2016) NIR-activated supersensitive drug release using nanoparticles with a flow core. Adv Funct Mater 26:7516–7525CrossRef Wang JX, Liu Y, Ma YC, Sun CY, Tao W, Wang YC, Yang XZ, Wang J (2016) NIR-activated supersensitive drug release using nanoparticles with a flow core. Adv Funct Mater 26:7516–7525CrossRef
38.
Zurück zum Zitat Zhang S, Chen H, Kong J (2016) Disulfide bonds-containing amphiphilic conetworks with tunable reductive-cleavage. RSC Adv 6:36568–36575CrossRef Zhang S, Chen H, Kong J (2016) Disulfide bonds-containing amphiphilic conetworks with tunable reductive-cleavage. RSC Adv 6:36568–36575CrossRef
39.
Zurück zum Zitat Duan X, Chen H, Fan L, Kong J (2016) Drug self-assembled delivery system with dual responsiveness for cancer chemotherapy. ACS Biomater Sci Eng 2:2347–2354CrossRef Duan X, Chen H, Fan L, Kong J (2016) Drug self-assembled delivery system with dual responsiveness for cancer chemotherapy. ACS Biomater Sci Eng 2:2347–2354CrossRef
40.
Zurück zum Zitat Dayyani N, Ramazani A, Khoee S, Shafiee A (2017) Synthesis and characterization of the first generation of polyamino-ester dendrimer-grafted magnetite nanoparticles from 3-aminopropyltriethoxysilane (APTES) via the convergent approach. Silicon 12:1–7 Dayyani N, Ramazani A, Khoee S, Shafiee A (2017) Synthesis and characterization of the first generation of polyamino-ester dendrimer-grafted magnetite nanoparticles from 3-aminopropyltriethoxysilane (APTES) via the convergent approach. Silicon 12:1–7
41.
Zurück zum Zitat Tarasi R, Khoobi M, Niknejad H, Ramazani A, Ma’mani L, Bahadorikhalili S, Shafiee A (2016) β-Cyclodextrin functionalized poly(5-amidoisophthalicacid) grafted Fe3O4 magnetic nanoparticles: a novel biocompatible nanocomposite for targeted docetaxel delivery. J Magn Magn Mater 417:451–459CrossRef Tarasi R, Khoobi M, Niknejad H, Ramazani A, Ma’mani L, Bahadorikhalili S, Shafiee A (2016) β-Cyclodextrin functionalized poly(5-amidoisophthalicacid) grafted Fe3O4 magnetic nanoparticles: a novel biocompatible nanocomposite for targeted docetaxel delivery. J Magn Magn Mater 417:451–459CrossRef
42.
Zurück zum Zitat An X, Zhu A, Luo H, Ke H, Chen H et al (2016) Rational design of multi-stimuli-responsive nanoparticles for precise cancer therapy. ACS Nano 10:5947–5958CrossRef An X, Zhu A, Luo H, Ke H, Chen H et al (2016) Rational design of multi-stimuli-responsive nanoparticles for precise cancer therapy. ACS Nano 10:5947–5958CrossRef
43.
Zurück zum Zitat Talelli M, Vicent MJ (2014) Reduction sensitive poly(l-glutamic acid) (PGA)-protein conjugates designed for polymer masked-unmasked protein therapy. Biomacromolecules 15:4168–4177CrossRef Talelli M, Vicent MJ (2014) Reduction sensitive poly(l-glutamic acid) (PGA)-protein conjugates designed for polymer masked-unmasked protein therapy. Biomacromolecules 15:4168–4177CrossRef
44.
Zurück zum Zitat Liu N, Vignolle J, Vincent J-M, Robert F, Landais Y et al (2014) One-pot synthesis and PEGylation of hyperbranched polyacetals with a degree of branching of 100%. Macromolecules 47:1532–1542CrossRef Liu N, Vignolle J, Vincent J-M, Robert F, Landais Y et al (2014) One-pot synthesis and PEGylation of hyperbranched polyacetals with a degree of branching of 100%. Macromolecules 47:1532–1542CrossRef
45.
Zurück zum Zitat Parmar RG, Busuek M, Walsh ES, Leander KR, Howell BJ et al (2013) Endosomolytic bioreducible poly(amido amine disulfide) polymer conjugates for the in vivo systemic delivery of siRNA therapeutics. Bioconjug Chem 24:640–647CrossRef Parmar RG, Busuek M, Walsh ES, Leander KR, Howell BJ et al (2013) Endosomolytic bioreducible poly(amido amine disulfide) polymer conjugates for the in vivo systemic delivery of siRNA therapeutics. Bioconjug Chem 24:640–647CrossRef
46.
Zurück zum Zitat Saptarshi C, Ramakrishnan S (2011) Hyperbranched polyacetals with tunable degradation rates. Macromolecules 44:4658–4664CrossRef Saptarshi C, Ramakrishnan S (2011) Hyperbranched polyacetals with tunable degradation rates. Macromolecules 44:4658–4664CrossRef
47.
Zurück zum Zitat Chen H, Jia J, Duan X, Yang Z, Kong J (2015) Reduction-cleavable hyperbranched polymers with limited intramolecular cyclization via click chemistry. J Polym Sci PolChem 53:2374–2380CrossRef Chen H, Jia J, Duan X, Yang Z, Kong J (2015) Reduction-cleavable hyperbranched polymers with limited intramolecular cyclization via click chemistry. J Polym Sci PolChem 53:2374–2380CrossRef
Metadaten
Titel
Amphiphilic polymer–drug conjugates based on acid-sensitive 100% hyperbranched polyacetals for cancer therapy
verfasst von
Xiao Duan
Yalan Wu
Mengsi Ma
Junjie Du
Shan Zhang
Heng Chen
Jie Kong
Publikationsdatum
01.05.2017
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 16/2017
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-017-1135-1

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