HomePolymer SynthesisFunctional Biomaterials Synthesized by Double-Head Polymerization Agents

Functional Biomaterials Synthesized by Double-Head Polymerization Agents

Hua Wei1, Suzie H. Pun2

1Lanzhou University, Lanzhou China, 2University of Washington


Over the past two decades, the rapid advance of controlled living polymerization (CLP) techniques, such as ring-opening polymerization (ROP),1 nitroxide-mediated polymerization (NMP),2 atom transfer free radical polymerization (ATRP),3 and reversible addition-fragmentation chain transfer (RAFT) polymerization,4 has enabled synthesis of welldefined polymers with controlled molecular weight and narrow molecular weight distribution (MWD) that are tailor-made for biomedical applications. There is an increasing demand for multifunctional synthetic polymers capable of interacting with, mimicking, or replacing natural materials for use in applications such as drug delivery, molecular imaging, cell therapy, and tissue engineering. One common strategy for the synthesis of multifunctional materials is to combine different synthetic techniques that involve complicated and multistep preparation and purification.5 The result, however, is often low reaction yield, batch-tobatch variation, and difficulties in scale-up. Thus, there is considerable need for simplified approaches to synthesis of polymers with advanced architectures and/or bioactive properties. This is particularly important for biomedical applications where simplified synthetic methods are advantageous for scale-up, manufacturing, and FDA approval. Doublehead polymerization agents have been developed to meet this demand and provide an elegant and robust approach to achieve this aim. These agents provide a nucleus that integrates different synthetic methods: e.g., CLP,1-4 click chemistry,6 and thiol chemistry.7

Double-head agents, (also called dual, bifunctional, or heterofunctional initiators) contain two functional sites capable of initiating concurrent polymerization independently and selectively. The use of double-head agents offers three advantages over conventional methods for polymer synthesis. The double-head agent: 1) provides an opportunity to prepare block copolymers in a concurrent, one-step manner without the need for intermediate transformation and protection steps, which is especially useful for the synthesis of block copolymers based on mechanistically incompatible monomers; 2) offers flexibility to the central bridge (block junction) connecting both functional ends that can be customized to meet the requirements for specific applications; and 3) affords two functional termini for the resulting block copolymer.

This review highlights recent progress in this field, with an emphasis on two types of double-head agents with symmetric and asymmetric structures, respectively (Table 1 on the following page). The preparation of polymers using these double-head agents and their biomedical applications are summarized in Figure 1. Finally, a perspective on the future direction of this rapidly developing research field is presented.

biomaterials synthesized

Figure 1. Examples of biomaterials synthesized using double-head agents covered in this review. Adapted with permission from the references as follows: Copyright (2013, 2011, 2008) American Chemical Society.20,22,29 Copyright (2006) John Wiley and Sons.9 Copyright (2010) Royal Society of Chemistry.25 Copyright (2013) Nature Publishing Group.

double head agents

Table 1.Summary of double-head agents with various structures.

Symmetrical Double-head Agents

Symmetrical double-head agents contain the same functional group at each end and are used to initiate simultaneous polymerization from both sides of the agent. These agents have been used to synthesize polymers with internal degradable bridges and also to incorporate functional termini in the cleaved polymer.

Tsarevsky and Matyjaszewski first reported the design of a degradable disulfide-bridged bifunctional ATRP initiator, bis[2-(2-bromopropionyloxy) ethyl] disulfide (BBPrEDS) (Prod. No. 723169) for the synthesis of degradable linear polystyrene (PS).8 Dithiothreitol (DTT) was used as a reducing agent to break the disulfide bridge and to obtain free thiolterminated PS with half the molecular weight of the parent polymer.

The BBPrEDS bifunctional initiator was used by Armes and co-workers to synthesize an ABA triblock copolymer by polymerizing first 2-(methacryloyloxy)ethyl phosphorylcholine (MPC) followed by N-isopropylacrylamide (NIPAAm), resulting in the PNIPAM80–PMPC125-SS-PMPC125–PNIPAM80 ABA triblock copolymer.9 This triblock copolymer formed a free-standing gel under physiologically relevant conditions at 37 °C and a copolymer concentration above approximately 8% (w/v). Cleavage of the central disulfide bond by biomolecules such as glutathione caused irreversible dissolution of the micellar gel. These copolymers constitute a new class of injectable gelators that are both biochemically responsive and thermo-responsive and could be useful as depots for localized drug or cell delivery.

Haddleton et al. reported the synthesis of two bifunctional ATRP initiators bearing Diels–Alder adducts—one based on a furan–maleimide adduct and the other based on an anthracene–maleimide adduct—which were used for the synthesis of linear poly(methyl methacrylate) (PMMA).10 The presence of the Diels–Alder adduct in the middle of the polymer chains allowed for their temperature-modulated reversible cleavage. These “selfhealing polymers” can be degraded by heating at high temperature and reformed by heating at lower temperature.

In another example, Zhao’s group developed a degradable disulfidebridged bifunctional RAFT chain transfer agent (CTA), S-cyanopentanoic acid dithiobenzoate (S-CPDB).11 In their study, RAFT and ROP were used with S-CPDB to prepare symmetric reduction-responsive amphiphilic star-like terpolymers. Upon redox stimuli and end-group modification, the resulting starlike terpolymers were efficiently converted into thiolfunctionalized telechelic stars, degraded miktoarm stars, and comb-like linear multiblock copolymers via various thiol modification reactions.

Bis(2-hydroxyethyl)disulfide (HES) (Prod. No. 380474) is a degradable disulfide-bridged bifunctional initiator that has been widely used to generate aliphatic polycarbonates by ROP of cyclic carbonates. Zhong et al. prepared poly(ethylene glycol)-b-PCL (PEG-SS-PCL) diblock copolymers by first synthesizing biodegradable poly(ε-caprolactone) disulfides, PCL-SS-PCL, through ROP of ε-caprolactone using HES initiator, reducing the polymers and reacting via disulfide exchange with PEG orthopyridyl disulfide.12 The reducible PEG-SS-PCL diblock copolymers were used for micellar delivery of the anticancer drug doxorubicin (Dox). Compared to a reduction-insensitive control material, the shell-sheddable micelles released Dox faster in the intracellular environment, resulting in higher anticancer efficacy.

Asymmetrical Double-head Agents

The synthesis of block copolymers based on mechanistically incompatible monomers using asymmetrical double-head agents has attracted considerable attention due to the simplified synthesis and the possibility of a concurrent, one-step process. The hetero double-head agent has two different functional groups that can perform two mechanistically different reactions/polymerizations without intermediate transformation steps. To obtain well-defined block copolymers using this agent via a one-step process, there should be no interactions between the two functional groups, catalysts or initiators, and monomers. In addition, the two polymerizations should proceed in a controlled manner at the same reaction temperature.13 Because of these limitations, most of the block copolymers synthesized using hetero double-head agents to date are prepared by a sequential reaction. This section reviews polymers synthesized using asymmetrical double-head agents with an emphasis on materials useful in biomedical applications.

ATRP Initiator-based Double-head Agents

The Maynard group employed a series of ATRP initiator-based doublehead agents in an elegant approach to prepare polymer-protein conjugates.14-16 In one study, a pyridyl disulfide (PDS)-modified ATRP initiator was used to prepare a well-defined poly(2-hydroxyethyl methacrylate) (P(HEMA)) that was then conjugated to bovine serum albumin.14 In the second report, a biotinylated ATRP initiator was bound to streptavidin and used as a protein macroinitiator for polymerization of NIPAAm.15 Finally, peptide macroinitiators were synthesized using amino acids with side-chain modified-ATRP initiators in solid-phase peptide synthesis. These macroinitiators were used to synthesize peptide-polymer (e.g., PHEMA and glycopolymers) conjugates exhibiting narrow molecular weight distributions, resulting in well-defined materials.16

Among the click chemistry group of reactions for facile coupling, the CuI-catalyzed azide-alkyne cycloaddition (CuAAC “click”)17 has received the most attention and has been increasingly employed in polymer functionalization and materials synthesis, especially in conjunction with controlled radical polymerization methods.18 The CuAAC “click” is particularly well-suited for pairing with ATRP, due to the ease of incorporating clickable functionality into polymers prepared by ATRP and the use of the same catalyst system in each process. The combination of these two powerful techniques has greatly expanded the range of available materials. In one example, the Grayson group used an alkynefunctionalized ATRP initiator to prepare cyclic polymers.19 Following this methodology, Wei et al. prepared cyclic cationic polymers for nucleic acid delivery and demonstrated that the cyclic polymers were just as effective in gene transfer but less cytotoxic to cultured mammalian cells compared with their linear analogues.20 Another useful agent was prepared by the Gohy and Fustin group; this ATRP initiator contained an o-nitrobenzyl ester photocleavable junction and an alkyne group for the CuAAC “click” reaction.21

Oh et al. prepared a reducible version of a double-head initiator (HO-SSiBuBr)22 for integrated ATRP and ROP techniques (HO-iBuBr, Prod. No. 723150)23 introduced by the Matyjaszewski group. In the presence of OH-SS-iBuBr, both ROP of lactide and ATRP of oligo(ethylene glycol) methyl ether methacrylate (OEGMA) were controlled, resulting in welldefined biodegradable block copolymers of PLA-SS-POEGMA with narrow MWD (<1.2). Aqueous micellization of PLA-SS-POEGMA resulted in core/shell micelles with SS links positioned at the interface between PLA cores and POEGMA coronas. In reducing environments such as the cytosol, POEGMA coronas were shed from the PLA cores, causing the precipitation of PLA core due to the loss of colloidal stability. These results, combined with non-cytotoxicity, indicated that the biodegradable PLA-based sheddable micelles could be useful as novel drug delivery systems for intracellular drug delivery.

Using this same double-head agent, Wei et al. synthesized a ternary, amphiphilic block copolymer PCL-SS-P((GMA-TEPA)-st-OEGMA) containing a sheddable hydrophobic PCL block, pH-sensitive oligoamine tetraethylenepentamine (TEPA)-decorated poly(glycidyl methacrylate) (PGMA) block, and a hydrophilic OEGMA segment.24 The sheddable hydrophobic PCL block was synthesized by ROP using the reducible double-head initiator HO-SS-iBuBr and then used as a macroinitiator for subsequent ATRP of GMA and OEGMA. This new block statistical copolymer combines reversible hydrophobization for enhanced particle stability in extracellular environments and statistical hydrophilization for efficient plasmid and siRNA release inside cells. This polymer was shown to be effective for in vivo gene transfer to mouse brain due to its multifunctional and bioresponsive properties.

RAFT CTA-based Double-head Agents

RAFT CTA-based double-head agents can be used to generate polymers with reactive termini for a variety of biomedical applications, including protein conjugation, nanoparticle grafting, and biofunctionalization. Zhao’s group reported novel strategies for combining RAFT polymerization and CuAAC “click” by using either a Z-azide-functionalized RAFT CTA, S-azidepropoxycarbonylethyl S’-methoxycarbonylphenylmethyl trithiocarbonate (AMP)25 or a Z-alkyne-functionalized RAFT CTA26 to prepare homopolymers and multiblock copolymers. These polymers were used for grafting to silica nanoparticles. The Maynard group designed a PDS-functionalized trithiocarbonate CTA for the preparation of protein-polymer conjugates.27 Covalent conjugation of a RAFTsynthesized heparin-mimicking polymer, poly(sodium 4-styrenesulfonateco-poly(ethylene glycol) methyl ether methacrylate) to basic fibroblast growth factor (bFGF) significantly enhanced protein stability under a variety of environmentally and therapeutically relevant stressors—such as heat, mild and harsh acidic conditions, storage and proteolytic degradation—different from native bFGF.

Advanced polymer structures also can be prepared using RAFT CTAbased double-head agents. Youk and co-workers synthesized welldefined block copolymers using 4-cyano-4-(dodecylsulfanylthiocarbonyl) sulfanylpentanol (CDP) as a dual initiator for RAFT polymerization and ROP in a one-step process.28 In one example, block copolymers with one block synthesized by RAFT polymerization of vinyl monomers and a second block synthesized by ROP of cyclic monomers were prepared in a one-step synthesis with selective catalysts for ROP that did not interfere with RAFT polymerization. RAFT polymerization in the presence of a compound capable of both reversible chain transfer through a thiocarbonylthio moiety and propagation via a vinyl group leads to highly branched copolymers. Sumerlin et al. synthesized an acryloyl trithiocarbonate and performed copolymerization with NIPAAm in ratios selected to control the distribution and length of branches in the resulting thermo-responsive copolymers.29 Retention of the active thiocarbonylthio compound during the polymerization was evidenced by a successfully subsequent chain extension of the resulting branched PNIPAAm macro-CTA by a further RAFT polymerization of a second monomer. This approach could be extendable to the synthesis of a variety of branched stimuli-responsive copolymers with a high concentration of sulfur-containing end groups that can facilitate polyvalent bioconjugation or surface immobilization.

RAFT–ATRP Double-head Agents

Wei et al. introduced a reducible RAFT–ATRP double-head agent for the synthesis of peptide-functionalized copolymers with sheddable shielding blocks for nucleic acid delivery applications.30 An optimized reduction-responsive cationic block copolymer, P(OEGMA)-SS-P(GMATEPA), was synthesized using this double-head agent by a combination of RAFT polymerization of OEGMA and ATRP of glycidyl methacrylate (GMA), followed by post-polymerization decoration of reactive epoxy groups in the P(GMA) block by tetraethylenepentamine (TEPA). The resulting diblock copolymer showed well-controlled composition with narrow MWD and was easily modified with a neuron targeting peptide, Tet1, at the outer corona by a Michael-type addition to the free thiols generated by aminolysis of the dithioester end group. The final polymer formed salt-stable particles amenable for in vivo use while maintaining high transfection efficiency, likely due to its multifunctional capabilities of targeting, endosomal escape, and deshielding and cargo release endowed by the Tet1 peptide, protonable TEPA amines, and reducible backbone structure, respectively (Figure 2). Thus, due to the combined properties of targeting and shielding, this block copolymer was shown to retain high transfection efficiencies comparable to the analogous homopolycation vectors for targeted gene delivery. The RAFT-ATRP double-head agent, therefore, provides a versatile means for preparing various types of multifunctional drug and gene delivery vehicles.

Pendant oligoamine side chain

Figure 2.Illustration for P(OEGMA)15-SS-P(GMA-TEPA)50 cationic polymer, DNA condensation, cell binding, endocytosis, and proposed route for subsequent reduction-triggered intracellular unpackage of pDNA. Copyright (2012) American Chemical Society.30

Conclusion and Perspective

The design and development of various double-head agents represent an elegant approach toward advanced materials design. With double-head agents, different polymerizations/reactions can be carried out without intermediate transformation and functionalization steps, sometimes even in a concurrent manner, significantly simplifying the traditional techniques for the preparation of block copolymers as well as generating a broad spectrum of novel block copolymers with fascinating properties based on diverse monomers. It is not surprising that the last decade has seen a tremendous growth in the development of such agents.

It is worth noting that the disulfide bond has attracted most of the attention, and it has been repeatedly employed as the degradable link in a double-head agent due to the excellent compatibility of disulfide with CLP processes, the reversible degradation and formation of the disulfide bond under mild conditions, and also the biological relevance of disulfides. Future research concerning the use of other stimuli-responsive links, such as acidic pH, temperature, enzyme-responsive substrates, and photo-sensitive bridges for the preparation of degradable double-head agents will be a hot topic and remains to be explored.

Looking to the future, much exciting work is expected to develop in the new field of advanced biomaterials prepared using various double-head agents.



Feng J, Zhuo R, Zhang X. 2012. Construction of functional aliphatic polycarbonates for biomedical applications. Progress in Polymer Science. 37(2):211-236.
Nicolas J, Guillaneuf Y, Lefay C, Bertin D, Gigmes D, Charleux B. 2013. Nitroxide-mediated polymerization. Progress in Polymer Science. 38(1):63-235.
Siegwart DJ, Oh JK, Matyjaszewski K. 2012. ATRP in the design of functional materials for biomedical applications. Progress in Polymer Science. 37(1):18-37.
Gregory A, Stenzel MH. 2012. Complex polymer architectures via RAFT polymerization: From fundamental process to extending the scope using click chemistry and nature's building blocks. Progress in Polymer Science. 37(1):38-105.
Chen J, Liu M, Gong H, Cui G, S, Gao C, Huang F, Chen T, Zhang X, Liu Z. 2013. Synthesis of linear amphiphilic tetrablock quaterpolymers with dual stimulus response through the combination of ATRP and RAFT by a click chemistry site transformation approach. Polym. Chem.. 4(6):1815.
Such GK, Johnston AP, Liang K, Caruso F. 2012. Synthesis and functionalization of nanoengineered materials using click chemistry. Progress in Polymer Science. 37(7):985-1003.
Roth PJ, Boyer C, Lowe AB, Davis TP. 2011. RAFT Polymerization and Thiol Chemistry: A Complementary Pairing for Implementing Modern Macromolecular Design. Macromol. Rapid Commun.. 32(15):1123-1143.
Tsarevsky NV, Matyjaszewski K. 2002. Reversible Redox Cleavage/Coupling of Polystyrene with Disulfide or Thiol Groups Prepared by Atom Transfer Radical Polymerization. Macromolecules. 35(24):9009-9014.
Li C, Madsen J, Armes SP, Lewis AL. 2006. A New Class of Biochemically Degradable, Stimulus-Responsive Triblock Copolymer Gelators. Angew. Chem. Int. Ed.. 45(21):3510-3513.
Syrett JA, Mantovani G, Barton WRS, Price D, Haddleton DM. 2010. Self-healing polymers prepared via living radical polymerisation. Polym. Chem.. 1(1):102.
Jiang X, Zhang M, Li S, Shao W, Zhao Y. 2012. Facile synthesis and versatile topological transformation of mono-cleavable symmetric starlike terpolymers. Chem. Commun.. 48(79):9906.
Sun H, Guo B, Cheng R, Meng F, Liu H, Zhong Z. 2009. Biodegradable micelles with sheddable poly(ethylene glycol) shells for triggered intracellular release of doxorubicin. Biomaterials. 30(31):6358-6366.
Bernaerts KV, Du Prez FE. 2006. Dual/heterofunctional initiators for the combination of mechanistically distinct polymerization techniques. Progress in Polymer Science. 31(8):671-722.
Bontempo D, Heredia KL, Fish BA, Maynard HD. 2004. Cysteine-Reactive Polymers Synthesized by Atom Transfer Radical Polymerization for Conjugation to Proteins. J. Am. Chem. Soc.. 126(47):15372-15373.
Bontempo D, Maynard HD. 2005. Journal of the American Chemical Society.(127):6508–6509.
Broyer RM, Quaker GM, Maynard HD. 2008. Designed Amino Acid ATRP Initiators for the Synthesis of Biohybrid Materials. J. Am. Chem. Soc.. 130(3):1041-1047.
Kolb HC, Finn MG, Sharpless KB. 2001. Angewandte Chemie International Edition.(40):2004–2021.
Barner-Kowollik C, Du?Prez FE, Espeel P, Hawker CJ, Junkers T, Schlaad H, Van?Camp W. 2011. ?Clicking? Polymers or Just Efficient Linking: What Is the Difference?. Angew. Chem. Int. Ed.. 50(1):60-62.
Laurent BA, Grayson SM. 2006. An Efficient Route to Well-Defined Macrocyclic Polymers via ?Click? Cyclization. J. Am. Chem. Soc.. 128(13):4238-4239.
Wei H, Chu DSH, Zhao J, Pahang JA, Pun SH. 2013. Synthesis and Evaluation of Cyclic Cationic Polymers for Nucleic Acid Delivery. ACS Macro Lett.. 2(12):1047-1050.
Schumers J, Gohy J, Fustin C. A versatile strategy for the synthesis of block copolymers bearing a photocleavable junction. Polym. Chem.. 1(2):161-163.
Khorsand Sourkohi B, Cunningham A, Zhang Q, Oh JK. 2011. Biodegradable Block Copolymer Micelles with Thiol-Responsive Sheddable Coronas. Biomacromolecules. 12(10):3819-3825.
Jakubowski W, Lutz J, Slomkowski S, Matyjaszewski K. 2005. Block and random copolymers as surfactants for dispersion polymerization. I. Synthesis via atom transfer radical polymerization and ring-opening polymerization. J. Polym. Sci. A Polym. Chem.. 43(7):1498-1510.
Wei H, Volpatti LR, Sellers DL, Maris DO, Andrews IW, Hemphill AS, Chan LW, Chu DSH, Horner PJ, Pun SH. 2013. Dual Responsive, Stabilized Nanoparticles for Efficient In?Vivo Plasmid Delivery. Angew. Chem. Int. Ed.. 52(20):5377-5381.
Huang Y, Hou T, Cao X, Perrier S, Zhao Y. 2010. Synthesis of silica-polymer hybrids by combination of RAFT polymerization and azide-alkyne cycloaddition ?click? reactions. Polym. Chem.. 1(10):1615.
Zhao G, Zhang P, Zhang C, Zhao Y. Facile synthesis of highly pure block copolymers by combination of RAFT polymerization, click reaction and de-grafting process. Polym. Chem.. 3(7):1803-1812.
Nguyen TH, Kim S, Decker CG, Wong DY, Loo JA, Maynard HD. 2013. A heparin-mimicking polymer conjugate stabilizes basic fibroblast growth factor. Nature Chem. 5(3):221-227.
Kang HU, Yu YC, Shin SJ, Youk JH. 2013. One?step synthesis of block copolymers using a hydroxyl?functionalized trithiocarbonate RAFT agent as a dual initiator for RAFT polymerization and ROP. J. Polym. Sci. A Polym. Chem.. 51(4):774-779.
Vogt AP, Sumerlin BS. 2008. Tuning the Temperature Response of Branched Poly(N-isopropylacrylamide) Prepared by RAFT Polymerization. Macromolecules. 41(20):7368-7373.
Wei H, Schellinger JG, Chu DSH, Pun SH. 2012. Neuron-Targeted Copolymers with Sheddable Shielding Blocks Synthesized Using a Reducible, RAFT-ATRP Double-Head Agent. J. Am. Chem. Soc.. 134(40):16554-16557.
Sign In To Continue

To continue reading please sign in or create an account.

Don't Have An Account?