Browsing by Author "Sarika, PR"

Now showing 1 - 8 of 8
  • Item
    A non-adhesive hybrid scaffold from gelatin and gum Arabic as packed bed matrix for hepatocyte perfusion culture
    (MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2015) Sarika, PR; Viha, CVS; Raj, RGS; Nirmala, RJ; Kumar, PRA
    Development of liver support systems has become one of the most investigated areas for the last 50 years because of the shortage of donor organs for orthotopic liver transplantations. Bioartificial liver (BAL) device is one of the alternatives for liver failure which provides a curing method and support patients to recover from certain liver failure diseases. The biological compartment of BAL is called the bioreactor where functionally active hepatocytes are maintained to support the liver specific functions. We have developed a packed bed bioreactor with a cytocompatible, polysaccharide protein hybrid scaffold. The scaffold prepared from gelatin and gum Arabic acts as a packed bed matrix for hepatocyte culture. Quantitative evaluation of the hepatocytes cultured using packed bed bioreactor demonstrated that cells maintained liver specific functions like albumin and urea synthesis for seven days. These results indicated that the system can be scaled up to form the biological component of a bioartificial liver. (C) 2014 Elsevier B.V. All rights reserved.
  • Item
    Galactosylated alginate-curcumin micelles for enhanced delivery of curcumin to hepatocytes
    (INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2016) Sarika, PR; James, NR; Kumar, PRA; Raj, DK
    Galactosylated alginate-curcumin conjugate (LANH(2)-Alg Ald-Cur) is synthesized for targeted delivery of curcumin to hepatocytes exploiting asialoglycoprotein receptor (ASGPR) on hepatocytes. The synthetic procedure includes oxidation of alginate (Alg), modification of lactobionic acid (LA), grafting of targeting group (modified lactobinic acid, LANH(2)) and conjugation of curcumin to alginate. Alginate-curcumin conjugate (Alg-Cur) without targeting group is also prepared for the comparison of properties. LANH(2)-Alg Ald-Cur self assembles to micelle with diameter of 235 +/- 5 nm and zeta potential of -29 mV in water. Cytotoxicity analysis demonstrates enhanced toxicity of LANH(2)-Alg Ald-Cur over Alg-Cur on HepG2 cells. Cellular uptake studies confirm that LANH(2)-Alg Ald-Cur can selectively recognize HepG2 cells and shows higher internalization than Alg-Cur conjugate. Results indicate that LANH(2)-Alg Ald-Cur conjugate micelles are suitable candidates for targeted delivery of curcumin to HepG2 cells. (C) 2016 Elsevier B.V. All rights reserved.
  • Item
    Galactosylated pullulan-curcumin conjugate micelles for site specific anticancer activity to hepatocarcinoma cells
    (COLLOIDS AND SURFACES B-BIOINTERFACES, 2015) Sarika, PR; James, NR; Nishna, N; Kumar, PRA; Raj, DK
    Galactosylated pullulan curcumin conjugate (LANH(2)-Pu Aid-Cur SA) is developed for target specific delivery of curcumin to hepatocarcinoma cells by five step synthetic strategy, which includes oxidation of pullulan (Pu Ald), introduction of amino group to the targeting ligand (LANH(2)), grafting of the LANH(2) to Pu Aid, modification of curcumin (Cur SA) and conjugation of Cur SA to pullulan. Nongalactosylated pullulan curcumin conjugate (Pu-Cur SA) is also prepared to compare the enhancement in cytotoxicity offered by the targeting group. Both LANH(2)-Pu Aid-Cur SA and Pu-Cur SA conjugates could self assemble to micelle in water with hydrodynamic diameters of 355 +/- 9 nm and 363 +/- 10 nm, respectively. Both conjugates show spherical morphology and enhance stability of curcumin in physiological pH. Compared to Pu-Cur SA, LANH(2)-Pu Aid-Cur SA exhibits higher toxicity and internalization towards HepG2 cells. This indicates the enhanced uptake of LANH(2)-Pu Ald-Cur SA conjugate via ASGPR (asialoglycoprotein receptor) mediated endocytosis into HepG2 cells. (C) 2015 Elsevier B.V. All rights reserved.
  • Item
    Gum arabic-curcumin conjugate micelles with enhanced loading for curcumin delivery to hepatocarcinoma cells
    (CARBOHYDRATE POLYMERS, 2015) Sarika, PR; James, NR; Kumar, PRA; Raj, DK; Kumary, TV
    Curcumin is conjugated to gum arabic, a highly water soluble polysaccharide to enhance the solubility and stability of curcumin. Conjugation of curcumin to gum arabic is confirmed by H-1 NMR, fluorescence and UV spectroscopy studies. The conjugate self assembles to spherical nano-micelles (270 +/- 5 nm) spontaneously, when dispersed in aqueous medium. Spherical morphology of the self assembled conjugate is evidenced by field emission scanning electron microscopy and transmission electron microscopy. The self assembly of the amphiphilic conjugate into micelle in aqueous medium significantly enhances the solubility (900 fold of that of free curcumin) and stability of curcumin in physiological pH. The anticancer activity of the conjugate micelles is found to be higher in human hepatocellular carcinoma (HepG2) cells than in human breast carcinoma (MCF-7) cells. The conjugate exhibits enhanced accumulation and toxicity in HepG2 cells due to the targeting efficiency of the galactose groups present in gum arabic. (C) 2015 Elsevier Ltd. All rights reserved.
  • Item
    Microgravity as a means to incorporate HepG2 aggregates in polysaccharide-protein hybrid scaffold
    (JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2016) Sarika, PR; James, NR; Anilkumar, PR; Raj, DK; Kumary, TV
    Tissue culture under microgravity provides a venue which promotes cell-cell association while avoiding the detrimental effects of high shear stress. Hepatocytes cultured on carriers or entrapped within matrices under simulated microgravity conditions showed improved cell function and proliferation. In the present study, a new approach was adopted where a non-cell adherent scaffold was incorporated with hepatospheroids (HepG2) under microgravity. Gum arabic (GA) was cross-linked with gelatin (GA-Gel) and collagen (GA-Col) to prepare non-cell adherent scaffolds. Microgravity experiments with GA-Gel and GA-Col indicated that GA-Col is a better substrate compared to GA-Gel. Microgravity experiments of GA-Col scaffolds with HepG2 cells confirmed that the non-adherent surface with porous architecture can incorporate hepatocyte spheroids and maintain liver specific functions. Albumin and urea synthesis of hepatocytes was sustained up to 6 days under microgravity conditions in the presence of GA-Col scaffold. This new approach of using non-cell adherent matrix and microgravity environment for developing biological substitutes will be beneficial in tissue engineering, bioartificial liver devices and in vitro safety assessment of drugs.
  • Item
    Modified gum arabic cross-linked gelatin scaffold for biomedical applications
    (MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2014) Sarika, PR; Cinthya, K; Jayakrishnan, A; Anilkumar, PR; James, NR
    The present work deals with development of modified gum arabic cross-linked gelatin scaffold for cell culture. A new biocompatible scaffold was developed by cross-linking gelatin (Gel) with gum arabic, a polysaccharide. Gum arabic was subjected to periodate oxidation to obtain gum arabic aldehyde (GAA). GAA was reacted with gelatin under appropriate pH to prepare the cross-linked hydrogel. Cross-linking occurred due to Schiff's base reaction between aldehyde groups of oxidized gum arabic and amino groups of gelatin. The scaffold prepared from the hydrogel was characterized by swelling properties, degree of cross-linking, in vitro degradation and scanning electron microscopy (SEM). Cytocompatibility evaluation using L-929 and HepG2 cells confirmed non-cytotoxic and non-adherent nature of the scaffold. These properties are essential for generating multicellular spheroids and hence the scaffold is proposed to be a suitable candidate for spheroid cell culture. (C) 2014 Elsevier B.V. All rights reserved.
  • Item
    Nanogels based on alginic aldehyde and gelatin by inverse miniemulsion technique: synthesis and characterization
    (CARBOHYDRATE POLYMERS, 2015) Sarika, PR; Kumar, PRA; Raj, DK; James, NR
    Nanogels were developed from alginic aldehyde and gelatin by an inverse miniemulsion technique. Stable inverse miniemulsions were prepared by sonication of noncontinuous aqueous phase (mixture of alginic aldehyde and gelatin) in a continuous organic phase (Span 20 dissolved in cyclohexane). Cross-linking occurred between alginic aldehyde (M) and gelatin (gel) in the presence of borax by Schiff's base reaction during the formation of inverse miniemulsion. The effects of surfactant (Span 20) concentration, volume of the aqueous phase and AA/gel weight ratio on the size of the alginic aldehyde-gelatin (AA-gel) nanoparticles were studied. Nanogels were characterized by DLS, FT-IR spectroscopy, TGA, SEM and TEM. DLS, TEM and SEM studies demonstrated nanosize and spherical morphology of the nanogels. Hemocompatibility and in vitro cytocompatibility analyses of the nanogels proved their nontoxicity. The results indicated the potential of the present nanogel system as a candidate for drug- and gene-delivery applications. (C) 2014 Elsevier Ltd. All rights reserved.
  • Item
    Preparation, characterization and biological evaluation of curcumin loaded alginate aldehyde-gelatin nanogels
    (MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2016) Sarika, PR; James, NR; Kumar, PRA; Raj, DK
    Curcumin, a natural polyphenol exhibits chemopreventive and chemotherapeutic activities towards cancer. In order to improve the bioavailability and therapeutic efficacy, curcumin is encapsulated in alginate aldehyde-gelatin (Alg Ald-Gel) nanogels. Alginate aldehyde-gelatin nanogels are prepared by inverse miniemulsion technique. Physicochemical properties of the curcumin loaded nanogels are evaluated by, Dynamic light scattering (DLS), NMR spectroscopy and Scanning electron microscopy (SEM). Curcumin loaded nanogels show hydrodynamic diameter of 431 +/- 8 nm and a zeta potential of 36 +/- 4 my. The prepared nanogels exhibit an encapsulation efficiency of 72 +/- 2%. In vitro drug release studies show a controlled release of curcumin from nanogels over a period of 48 h. Hemocompatibility and cytocompatibility of the nanogels are evaluated. Bare nanogels are cytocompatible and curcumin loaded nanogels induce anticancer activity towards MCF-7 cells. In vitro cellular uptake of the curcumin loaded nanogels using confocal laser scanning microscopy (CLSM) confirms the uptake of nanogels in MCF-7 cells. Hence, the developed nanogel system can be a suitable candidate for curcumin delivery to cancer cells. (C) 2016 Elsevier B.V. All rights reserved.