Polymeric micelles are virus-sized with a core-shell structure having a hydrophobic core and a hydrophilic shell and, more significantly, inherent stealth. Polymeric micelles seem ideal for the targeted and Eltanexor mouse controlled delivery of hydrophobic anticancer drugs, including paclitaxel and doxorubicin [4], in that they significantly increase their water solubility, extend their circulation time, passively target tumor tissues [5], increase their bioavailability, have tremendous biocompatibility, and are degradable in vivo into nontoxic products. Several types of polymer blocks can be used to form micelles, of which the most studied include poly(α-hydroxy esters) [6] (such as polylactide [7], polyglycolide

[8], and poly(ε-caprolactone) [9]), Bafilomycin A1 research buy polyether [10], hydrotrophic polymers [11], and poly(amino acids) [12]. Several attempts have been made to formulate stable polymeric micelles with new surfactant combinations to achieve ideal drug delivery in vitro

as well as in vivo. Cholic acid (CA), a bile acid, is an amphiphilic steroid molecule naturally synthesized from cholesterol, which organizes into micelles above the critical micelle concentration (CMC). Bile acids, together with the phospholipids, vary the permeability of cell membranes [13]. Some bile acids form hydrogen-bonded aggregates with some drugs, which may lead to alterations in drug bioavailability [14]. Polyethyleneimine (PEI) is a cationic synthetic vector mainly used for gene delivery owing to its high nucleic acid condensing potential, ability to escape endosomes [15], nuclear localization capability [16], find protocol and promising transfection efficacy both in vitro and in vivo[15]. We synthesized doxorubicin-loaded cholic acid-polyethyleneimine (CA-PEI) micelles as an antitumor drug delivery system. The antitumor activity of the doxorubicin-loaded Axenfeld syndrome CA-PEI micelles was then tested using human colorectal adenocarcinoma (DLD-1) cells. Methods Materials CA, PEI (average molecular

weight (MW) approximately 1,300), N,N’-dicyclohexylcarbodiimide (DCC), N-hydroxysuccinimide (NHS), hydrochloric acid (HCl), triethylamine, tetrahydrofuran, and dichloromethane were purchased from Sigma-Aldrich (St. Louis, MO, USA). Doxorubicin was purchased from Calbiochem (Merck KGaA, Darmstadt, Germany). The Spectra/Por™ dialysis membrane (MW cutoff (MWCO) = 1,000 g/mol) was purchased from Spectrum Labs (Rancho Dominguez, CA, USA). Synthesis of the CA-PEI copolymer The side-chain carboxyl group at the C-24 position in CA was conjugated to the terminal amine group of PEI. This was carried out by dissolving CA in tetrahydrofuran and activating it with DCC and NHS at 25°C for 8 h. CA was then precipitated in ice-cold n-hexane and dried in an oven at 40°C for 2 h. The activated CA was then conjugated to the primary amine group of PEI by incubating for 15 h in dichloromethane (Figure 1) using CA-PEI molar ratios of 1:1, 1:2, 1:4, 3:1, and 4:1.