Self-assembled peptide (CADY-1) improved the clinical application of doxorubicin.

CADY-1 is an amphipathic peptide that possesses cell-penetrating activity. As an amphipathic peptide, CADY-1 is capable of forming complexes by self-assembly, and they are these complexes that possess cell-penetrating activity. This distinct characteristic of CADY-1 makes it a potent cell-penetrating drug delivery system. Doxorubicin is a widely used cytotoxic anti-cancer drug but is limited by its toxicity. Although the liposomal formulation of doxorubicin ameliorates its toxicity, its complicated synthesis remains an obstacle to its wide clinical use. In this study, our findings revealed that CADY-1 and doxorubicin form a stable complex at optimised molar ratios in a self-assembling manner. Formation of the complex extended the blood residence time of doxorubicin in a similar fashion to that of liposomal doxorubicin. In addition, the complex was capable of carrying doxorubicin across the cell membrane, which increased the therapeutic index of doxorubicin. Experimental animals treated with a CADY-1/doxorubicin complex exhibited better tolerance and anti-tumour activity than animals treated with either liposomal doxorubicin or the free form of doxorubicin. Collectively, the findings in this study support the advantages of using complexes formed by the self-assembled peptide CADY-1 and suggest that CADY-1 is a potent drug delivery system.

[1]  Li Zhang,et al.  Direct comparison of two pegylated liposomal doxorubicin formulations: is AUC predictive for toxicity and efficacy? , 2007, Journal of controlled release : official journal of the Controlled Release Society.

[2]  Z. Pavelic,et al.  Preclinical toxicology study of liposome encapsulated doxorubicin (TLC D-99): comparison with doxorubicin and empty liposomes in mice and dogs. , 1993, In vivo.

[3]  A. Kichler,et al.  Self-promoted cellular uptake of peptide/DNA transfection complexes. , 2007, Biochemistry.

[4]  S. Carter Adriamycin-a review. , 1975, Journal of the National Cancer Institute.

[5]  F. Hudecz,et al.  Medium‐sized peptides as built in carriers for biologically active compounds , 2005, Medicinal research reviews.

[6]  Yuquan Wei,et al.  Improving anticancer activity and reducing systemic toxicity of doxorubicin by self-assembled polymeric micelles , 2011, Nanotechnology.

[7]  A. Ballestrero,et al.  Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. , 2004, Journal of molecular and cellular cardiology.

[8]  Y. Li,et al.  Peptide complex containing GLP-1 exhibited long-acting properties in the treatment of type 2 diabetes. , 2011, Diabetes research and clinical practice.

[9]  Y. Barenholz,et al.  Enhancement of adriamycin delivery to liver metastatic cells with increased tumoricidal effect using liposomes as drug carriers. , 1983, Cancer research.

[10]  E. Gazit,et al.  Controlled patterning of aligned self-assembled peptide nanotubes , 2006, Nature nanotechnology.

[11]  H. Shmeeda,et al.  Pros and Cons of the Liposome Platform in Cancer Drug Targeting , 2006, Journal of liposome research.

[12]  Y. Li,et al.  Application of novel peptide (Pp1) improving the half-life of exendin-4 in vivo , 2011, Peptides.

[13]  M S Sachdeva,et al.  Drug targeting systems for cancer chemotherapy. , 1998, Expert opinion on investigational drugs.

[14]  M. Morris,et al.  Peptide-based nanoparticle for ex vivo and in vivo drug delivery. , 2008, Current pharmaceutical design.

[15]  R. Brasseur,et al.  A new potent secondary amphipathic cell-penetrating peptide for siRNA delivery into mammalian cells. , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

[16]  Annick Thomas,et al.  Insight into the cellular uptake mechanism of a secondary amphipathic cell-penetrating peptide for siRNA delivery. , 2010, Biochemistry.

[17]  E. Giralt,et al.  Amphipathic peptides and drug delivery. , 2004, Biopolymers.

[18]  P S Schein,et al.  Prevention of chronic doxorubicin cardiotoxicity in beagles by liposomal encapsulation. , 1983, Cancer research.

[19]  Lijuan Chen,et al.  Poly(epsilon-caprolactone)-poly(ethylene glycol)-poly(epsilon-caprolactone) (PCL-PEG-PCL) nanoparticles for honokiol delivery in vitro. , 2009, International journal of pharmaceutics.

[20]  M. Bally,et al.  Characterization of liposomal systems containing doxorubicin entrapped in response to pH gradients. , 1990, Biochimica et biophysica acta.

[21]  P. Oliveira,et al.  Carvedilol-mediated antioxidant protection against doxorubicin-induced cardiac mitochondrial toxicity. , 2004, Toxicology and applied pharmacology.

[22]  R. Shohet,et al.  Transcriptional analysis of doxorubicin-induced cardiotoxicity. , 2006, American journal of physiology. Heart and circulatory physiology.

[23]  Satoko Mizuno,et al.  A New Antitumor Agent Amrubicin Induces Cell Growth Inhibition by Stabilizing Topoisomerase II‐DNA Complex , 1998, Japanese journal of cancer research : Gann.

[24]  Xian‐Zheng Zhang,et al.  Novel vesicles self-assembled from amphiphilic star-armed PEG/polypeptide hybrid copolymers for drug delivery. , 2011, Macromolecular bioscience.

[25]  A. Falanga,et al.  Intracellular delivery: exploiting viral membranotropic peptides. , 2012, Current drug metabolism.