Fabrication of Mn-TPP/RGO Tailored Glassy Carbon Electrode for Doxorubicin Sensing.

Cancer is a long-standing disease, and the use of anticancer drugs can cause many different harmful side effects. Therefore, the quantitative analysis of anticancer drugs is crucial. Among all the analytical techniques that have been utilized for the detection of doxorubicin, electrochemical sensors have drawn exceptional consideration because they are simple, affordable, and highly sensitive. Manganese tetraphenylporphyrin decorated reduced graphene oxide (Mn-TPP/RGO), tetraphenylporphyrin decorated reduced graphene oxide (TPP/RGO), and reduced graphene oxide (RGO) nanostructure based glassy carbon electrodes (GCEs) were fabricated for the detection of doxorubicin (DOX). The synthesized materials were characterized by FTIR, scanning electron microscopy (SEM), ultraviolet-visible spectroscopy (UV/vis), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). Doxorubicin detection was performed using differential pulse voltammetry (DPV), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). Among the prepared electrodes, Mn-TPP/RGO modified GCE gave an optimum peak current at pH 3. The Mn-TPP/RGO modified electrode showed significant linear response range (0.1-0.6 mM); effective sensitivity (112.09 µA mM-1 cm-2); low detection limit (63.5 µM); and excellent stability, selectivity, repeatability, and reproducibility toward doxorubicin. With differential pulse voltammetry, LoD and sensitivity were 27 µM and 0.174 µA µM-1 cm-2, respectively. Real sample analysis was also performed in human serum, and it depicted reasonable recovery results for spiked doxorubicin.

Enhanced removal of toxic Cr(vi) and Pb(ii) from water using carboxylic terminated Ti3C2Tx nanosheets.

The discharge of Cr(vi)and Pb(ii) contaminants into water resources through industrial waste induces a considerable risk to human and marine life, which demands an effective removal of these toxic metal ions (MI) from the aquatic environment. This study presents a remarkable adsorption performance of the carboxylic terminated Ti3C2Tx nanosheets synthesized using ammonium bifluoride and citric acid and applied as adsorbents for the removal of Cr(vi)and Pb(ii) from water. Adsorption efficiency was evaluated under sonication, MI concentration, and solution temperature at pH 5.5. Maximum adsorption capacities of 1090 mg g-1 and 1135 mg g-1 for Cr(vi) and Pb(ii) were attained within 7 and 4 minutes, respectively. Moreover, adsorption kinetic and isotherm studies were conducted, and the experimental data was found to fit well with pseudo-second-order reaction and Freundlich models. It was also established that the main interactions to drive the adsorption reactions were the electrostatic forces between the adsorbates and Ti3C2Tx adsorbent. Furthermore, (-COOH) and (-OH) terminal groups were the main contributors to the adsorption of Cr(vi) and Pb(ii) pollutants through an ion exchange mechanism. Besides the ion exchange mechanism, chemical coordination, entrapment of the adsorbates, and van der Waals forces lead to a physiochemical interaction between the MI and Ti3C2Tx nanosheets. In addition, Ti3C2Tx nanosheets showed better selectivity towards Pb(ii) removal than Cr(vi) in an aqueous solution. The nanosheets also exhibited more than 80% removal efficiency even after six cycles of regeneration and reusability. Additionally, Ti3C2Tx nanosheets offered superior adsorption performance for Cr(vi) and Pb(ii) compared to previously reported titanium carbide MXenes and activated carbon-based adsorbents. Hence, these high-quality and efficient Ti3C2Tx nanosheets can potentially eradicate other hazardous MI contaminants from wastewater.

Antifouling and Water Flux Enhancement in Polyethersulfone Ultrafiltration Membranes by Incorporating Water-Soluble Cationic Polymer of Poly [2-(Dimethyl amino) ethyl Methacrylate].

Novel ultrafiltration (UF) polymer membranes were prepared to enhance the antifouling features and filtration performance. Several ultrafiltration polymer membranes were prepared by incorporating different concentrations of water-soluble cationic poly [2-(dimethyl amino) ethyl methacrylate] (PDMAEMA) into a homogenous casting solution of polyethersulfone (PES). After adding PDMAEMA, the effects on morphology, hydrophilicity, thermal stability, mechanical strength, antifouling characteristics, and filtration performance of these altered blended membranes were investigated. It was observed that increasing the quantity of PDMAEMA in PES membranes in turn enhanced surface energy, hydrophilicity, and porosity of the membranes. These new modified PES membranes, after the addition of PDMAEMA, showed better filtration performance by having increased water flux and a higher flux recovery ratio (FRR%) when compared with neat PES membranes. For the PES/PDMAEMA membrane, pure water flux with 3.0 wt.% PDMAEMA and 0.2 MPa pressure was observed as (330.39 L·m-2·h-1), which is much higher than that of the neat PES membrane with the value of (163.158 L·m-2·h-1) under the same conditions. Furthermore, the inclusion of PDMAEMA enhanced the antifouling capabilities of PES membranes. The total fouling ratio (TFR) of the fabricated PES/PDMAEMA membranes with 3.0 wt.% PDMAEMA at 0.2 MPa applied pressure was 36 percent, compared to 64.9 percent for PES membranes.

Probing the behavior and kinetic studies of amphiphilic acrylate copolymers with bovine serum albumin.

This article presents that acrylate copolymers are the potential candidate against the adsorption of bovine serum albumin (BSA). A series of copolymers poly(methyl methacrylate) (pMMA), poly(3-sulfopropyl methacrylate-co-methyl methacrylate) p(SPMA-co-MMA), and poly(dimethylaminoethyl methacrylate-co-methyl methacrylate) p(DMAEMA-co-MMA) were synthesized via free radical polymerization. These amphiphilic copolymers are thermally stable with a glass transition temperature (Tg) 50-120 °C and observed the impact of surface charge on amphiphilic copolymers to control interactions with the bovine serum albumin (BSA). These copolymers pMD1 and pMS1 have surface charges, - 56.6 and - 72.6 mV at pH 7.4 in PBS buffer solution that controls the adsorption capacity of bovine serum albumin (BSA) on polymers surface. Atomic force microscopy (AFM) analysis showed minimum roughness of 0.324 nm and 0.474 nm for pMS1 and pMD1. Kinetic studies for BSA adsorption on these amphiphilic copolymers showed the best fitting of the pseudo-first-order model that showed physisorption and attained at 25 °C and pH 7.4 within 24 h.

Layer-By-Layer Self-Assembled Dip Coating for Antifouling Functionalized Finishing of Cotton Textile.

The fouling of surfaces such as textiles is a major health challenge, and there is a continuous effort to develop materials and processes to overcome it. In consideration of this, this study regards the development of antifouling functional nanoencapsulated finishing for the cotton textile fabric by employing a layer-by-layer dip coating technique. Antifouling textile finishing was formulated by inducing the nanoencapsulation of the antifouling functional group inside the hydrophobic polymeric shell. Cotton fabric was taken as a substrate to incorporate antibacterial functionality by alternatively fabricating multilayers of antifouling polymeric formulation (APF) and polyelectrolyte solution. The surface morphology of nanoencapsulated finished textile fabric was characterized through scanning electron microscopy to confirm the uniform distribution of nanoparticles on the cotton textile fabric. Optical profilometry and atomic force microscopy studies indicated increased surface roughness in the coated textile substrate as compared to the uncoated textile. The surface thickness of the fabricated textile increased with the number of deposited bilayers on the textile substrate. Surface hydrophobicity increased with number of coating bilayers with θ values of x for single layer, up to y for 20 bilayers. The antibacterial activity of the uncoated and layer-by-layer coated finished textile was also evaluated. It was significant and exhibited a significant zone of inhibition against microbial strains Gram-positive S. aureus and Gram-negative E. coli. The bilayer coating exhibited water repellency, hydrophobicity, and antibacterial activity. Thus, the fabricated textile could be highly useful for many industrial and biomedical applications.

Development of Ag0.04ZrO2/rGO heterojunction, as an efficient visible light photocatalyst for degradation of methyl orange.

Methyl orange (MO) is mutagenic, poisonous, and carcinogenic in nature, hence, effective methods are required for its degradation. We have synthesized pure ZrO2, Ag-doped ZrO2, and Ag-doped ZrO2/rGO as hybrid photocatalysts by facile hydrothermal method. These photocatalysts were characterized by powder XRD, scanning electron microscopy, EDX, FTIR, photoluminescence, UV-Vis diffuse reflectance (DRS), and Raman spectroscopy. The photodegradation of MO (10 ppm) was studied with pure ZrO2, Ag-doped ZrO2, and Ag-doped ZrO2/rGO (10 mg/100 mL catalyst dosage) photocatalysts at 100 min irradiation time under UV-Visible light. The pH effect and catalyst dosage on photodegradation of MO was investigated. Ag0.04ZrO2/rGO photocatalyst exhibited the maximum photocatalytic degradation of MO (87%) as compared to Ag0.04ZrO2 (60%) and pure ZrO2 (26%). Reusability experiments ensured the excellent stability of photocatalyst after five consecutive experiments. To the best of our knowledge, this is the first report on the facile hydrothermal synthesis of Ag0.04ZrO2/rGO photocatalyst for photocatalytic degradation of methyl orange.

Efficient photocatalytic degradation of nitrobenzene by copper-doped TiO2: kinetic study, degradation pathway, and mechanism.

Cu-doped TiO2 (0.1, 0.25, and 0.5% Cu-TiO2) photocatalyst was prepared by sol-gel method and was characterized by powder XRD, FTIR, TEM, SEM, EDX, UV-vis diffuse reflectance (DRS), photoluminescence (PL), and Raman spectroscopy. The XRD spectrum shows tetragonal anatase phase. TEM analysis indicate that the nanoparticles were spherical with sizes 12-13 nm. The degradation of NB was studied, and an optimal degradation time of 180 min led to 98.6% NB abatement of NB = 0.05 mM, pH = 4, and catalyst loading = 50 mg/100 mL, under visible light. The degradation of NB follows the pseudo-first-order kinetics. The reusability studies indicated the excellent stability of 0.25% Cu-TiO2.

Cefotaxime Loaded Polycaprolactone Based Polymeric Nanoparticles with Antifouling Properties for In-Vitro Drug Release Applications.

The objective of the present study was to achieve the successful encapsulation of a therapeutic agent to achieve antifouling functionality regarding biomedical applications. Considering nanotechnology, drug-loaded polycaprolactone (PCL)-based nanoparticles were prepared using a nano-precipitation technique by optimizing various process parameters. The resultant nano-formulations were investigated for in vitro drug release and antifouling applications. The prepared particles were characterized in terms of surface morphology and surface properties. Optimized blank and drug-loaded nanoparticles had an average size of 200 nm and 216 nm, respectively, with associated charges of -16.8 mV and -11.2 mV. Studies of the in vitro release of drug were carried out, which showed sustained release at two different pH, 5.5 and 7.4 Antifouling activity was observed against two bacterial strains, Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli. The zone of inhibition of the optimized polymeric drug-loaded nanoparticle F-25 against both strains were compared with the pure drug. The gradual pH-responsive release of antibiotics from the biodegradable polymeric nanoparticles could significantly increase the efficiency and pharmacokinetics of the drug as compared to the pure drug. The acquired data significantly noted that the resultant nano-encapsulation of antifouling functionality could be a promising candidate for topical drug delivery systems and skin applications.

Electrocatalytic performance of NiNH2BDC MOF based composites with rGO for methanol oxidation reaction.

Present work comprehensively investigated the electrochemical response of Nickel-2 Aminoterephthalic acid Metal-Organic Framework (NiNH2BDC) and its reduced graphitic carbon (rGO) based hybrids for methanol (CH3OH) oxidation reaction (MOR) in an alkaline environment. In a thorough analysis of a solvothermally synthesized Metal-Organic Frameworks (MOFs) and its reduced graphitic carbon-based hybrids, functional groups detection was performed by FTIR, the morphological study by SEM, crystal structure analysis via XRD, and elemental analysis through XPS while electrochemical testing was accomplished by Chronoamperometry (CA), Cyclic Voltametric method (CV), Electrochemically Active Surface Area (EASA), Tafel slope (b), Electron Impedance Spectroscopy (EIS), Mass Activity, and roughness factor. Among all the fabricated composites, NiNH2BDC MOF/5 wt% rGO hybrid by possessing an auspicious current density (j) of 267.7 mA/cm2 at 0.699 V (vs Hg/HgO), a Tafel slope value of 60.8 mV dec-1, EASA value of 15.7 cm2, and by exhibiting resistance of 13.26 Ω in a 3 M CH3OH/1 M NaOH solution displays grander electrocatalytic activity as compared to state-of-the-art platinum-based electrocatalysts.

Supramolecular assemblies of carbon nanocoils and tetraphenylporphyrin derivatives for sensing of catechol and hydroquinone in aqueous solution.

Non-enzymatic electrochemical detection of catechol (CC) and hydroquinone (HQ), the xenobiotic pollutants, was carried out at the surface of novel carbon nanocoils/zinc-tetraphenylporphyrin (CNCs/Zn-TPP) nanocomposite supported on glassy carbon electrode. The synergistic effect of chemoresponsive activity of Zn-TPP and a large surface area and electron transfer ability of CNCs lead to efficient detection of CC and HQ. The nanocomposite was characterized by using FT-IR, UV/vis. spectrophotometer, SEM and energy dispersive X-ray spectroscopy (EDS). Cyclic voltammetry, differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy were used for the electrochemical studies. CNCs/Zn-TPP/GCE nanosensor displayed a limit of detection (LOD), limit of quantification (LOQ) and sensitivity for catechol as 0.9 µM, 3.1 µM and 0.48 µA µM-1 cm-2, respectively in a concentration range of 25-1500 µM. Similarly, a linear trend in the concentration of hydroquinone detection was observed between 25 and 1500 µM with an LOD, LOQ and sensitivity of 1.5 µM, 5.1 µM and 0.35 µA µM-1 cm-2, respectively. DPV of binary mixture pictured well resolved peaks with anodic peak potential difference, ∆Epa(CC-HQ), of 110 mV showing efficient sensing of CC and HQ. The developed nanosensor exhibits stability for up to 30 days, better selectivity and good repeatability for eight measurements (4.5% for CC and 5.4% for HQ).

Synthesis, characterization and catalytic testing of MCM-22 derived catalysts for n-hexane cracking.

Layered zeolites and their delaminated structures are novel materials that enhance the catalytic performance of catalysts by addressing diffusion limitations of the reactant molecules. n-Hexane catalytic cracking was observed over MCM-22 layered zeolite and its derivative structures over the temperature range of 450-650 °C for the production of olefins. MCM-22, H-MCM-22, and ITQ-2 zeolites were prepared by the hydrothermal method. Oxalic acid was used as a dealuminating reagent to obtain H-MCM-22 with various Si/Al ratios ranging from 09-65. The prepared samples were characterized by XRD, SEM, TGA, and BET. The cracking of n-hexane was carried out by Pyro/GC-MS. It was observed that the selectivity for olefins was improved by increasing the Si/Al ratio. H-MCM-22-10% produced the highest relative olefinic concentration of 68% as compared to other dealuminated structures. Moreover, the product distribution showed that higher reaction temperature is favorable to produce more olefins. Furthermore, a comparison between ITQ-2 and MCM-22 derived structures showed that ITQ-2 is more favorable for olefins production at high temperatures. The concentration of relative olefins was increased up to 80% over ITQ-2 at 650 °C.

Efficient Photoelectrochemical Water Splitting by Tailoring MoS2/CoTe Heterojunction in a Photoelectrochemical Cell.

Solar energy conversion through photoelectrochemical water splitting (PEC) is an upcoming promising technique. MoS2/CoTe heterostructures were successfully prepared and utilized for PEC studies. MoS2 and CoTe were prepared by a hydrothermal method which were then ultrasonicated with wt. % ratios of 1:3, 1:1 and 3:1 to prepare MoS2/CoTe (1:3), MoS2/CoTe (1:1) and MoS2/CoTe (3:1) heterostructure, respectively. The pure materials and heterostructures were characterized by XRD, UV-vis-DRS, SEM, XPS, PL and Raman spectroscopy. Photoelectrochemical measurements were carried out by linear sweep voltammetry and electrochemical impedance spectroscopic measurements. A maximum photocurrent density of 2.791 mA/cm2 was observed for the MoS2/CoTe (1:1) heterojunction which is about 11 times higher than the pristine MoS2. This current density was obtained at an applied bias of 0.62 V vs. Ag/AgCl (1.23 V vs. RHE) under the light intensity of 100 mW/cm2 of AM 1.5G illumination. The enhanced photocurrent density may be attributed to the efficient electron-hole pair separation. The solar to hydrogen conversion efficiency was found to be 0.84% for 1:1 MoS2/CoTe, signifying the efficient formation of the p-n junction. This study offers a novel heterojunction photocatalyst, for PEC water splitting.

Nanocomposites of NiO/CuO Based MOF with rGO: An Efficient and Robust Electrocatalyst for Methanol Oxidation Reaction in DMFC.

In this work a novel bimetallic nickel oxide/copper oxide metal-organic framework (NiO/CuO MOF) has been developed by using two linkers: Benzene Dicarboxylic acid (BDC) and Pyrazine. The composites of NiO/CuO MOF with different amounts of reduced graphene oxide (rGO) were synthesized through a hydrothermal method and subsequently characterized by multiple significant techniques like XRD, SEM, EDX, FTIR and Raman IR for an investigation of their structural and morphological properties. The prepared series of material was later employed for electrochemical oxidation of methanol, tested by cyclic voltammetry (CV) in basic medium on a modified glassy carbon electrode (GCE). The electrochemical response depicts that increasing concentration of rGO enhances the electrocatalytic activity of the catalyst for methanol oxidation reaction (MOR). The catalyzed oxidation reaction of methanol by NiO/CuO MOF and rGO-NiO/CuO MOF composites give a superlative current density of 437. 28 mA/cm2 at 0.9 V potential at 50 mV/s scan rate. This activity makes it a promising catalytic material for electrolysis of methanol in direct methanol fuel cell (DMFC).

Methanol outbreak in the district of Hulu Langat, 2018

@#Introduction: A methanol outbreak occurred in the district of Hulu Langat on 16 September 2018. The Hulu Langat District Health Office received 25 notifications of a suspected methanol poisoning from Kajang and Ampang Hospital. An outbreak investigation was done to determine the source followed by a preventive and control measure. Method: Active case detection was done on cases living quarters and workplaces. Patients were interviewed, and their blood and urine samples were sent for methanol analysis. Samples of suspected alcoholic beverages were also sent for analysis. A suspected case was defined as any person presented with clinical symptoms with a history of consuming alcoholic beverages within five days before symptoms and high anion gap metabolic acidosis. A confirmed case was defined as a suspected case with positive blood and urine methanol. Results: In total, there were 25 suspected cases, of which 12 cases were confirmed. The calculated attack rate was 48%. There were six mortalities (50%) secondary to severe metabolic acidosis. The most common presenting symptom was vomiting (75%) and abdominal pain (41.7%). These cases were linked to consumption of illicitly produced alcohol. Samples of the alcoholic drinks were positive containing high level of methanol. Conclusion: The methanol outbreak in the Hulu Langat was successfully managed. Appropriate control and prevention measures were taken, including health promotion and joint enforcement activities. Steps were taken successfully through collaborations with multiple agencies and cooperation with Selangor Health Departments and the Ministry of Health. Continuous surveillance on the product of liquor, and health promotion are essential to prevent a similar outbreak from happening again in future.

A super stretchable and sensitive strain sensor based on a carbon nanocoil network fabricated by a simple peeling-off approach.

Despite the tremendous progress in wearable and smart strain sensors, it is still a challenge to develop a highly sensitive, stretchable, and low-cost sensor. Herein, a super stretchable and sensitive strain sensor fabricated by a simple peeling-off approach is reported. The strain sensor is prepared by peeling off a thin as-grown carbon nanocoil (CNC) film from a substrate using a stretchable polydimethylsiloxane (PDMS) film or a flexible adhesive tape. Herein, we took advantage of the spring-like morphology and the original network of the CNCs. The sensor is used to detect pressure, tension, and bend. The strain range and maximum real-time gauge factor reach 260% and 190, respectively, with a rapid response time (less than 12 ms). The contrary resistance responses under tension and bend make it possible to distinguish the direction and type of strain. The sensor is used to monitor a strain over a wide range, from human pulse to the impact of a 0.9 kg weight. The high sensitivity and stretchability, easy and cheap fabrication, and effective interaction with human motions suggest the great potential applications of this sensor in wearable strain sensors and smart systems.

A flexible, ultra-sensitive strain sensor based on carbon nanocoil network fabricated by an electrophoretic method.

An ultra-sensitive strain sensor has been fabricated and studied, whose sensing medium is a network structure composed of plenty of carbon nanocoils (CNCs) and deposited between two gold electrodes via electrophoresis. The sensor owns a gauge factor close to 10 000 for tensile strain. A high stability and reproducibility of more than 5000 cycles and a fast response time of approximately 50 ms have been achieved. It has a high sensitivity for bending strain as well. Practically, it has shown an excellent performance in the detection of breathing, wrist pulse, and vibration. The sensor can be fabricated with a facile technology and low cost, suggesting great potential applications in micro-nano electromechanical systems, wearable devices and electronic skins.

Effect of trihalomethanes (chloroform and bromoform) on human haematological count.

With the increasing concerns about the harmful effects of disinfection products, the process of chlorination is becoming questionable. Bromoform and chloroform are among the most frequently occurring disinfection by-products. Haematological parameters are an important indicator of human well-being which is why the prime objective of the current study was to conduct a dose-response assessment to investigate the effects of trihalomethanes on human haematological count. Blood samples of healthy subjects were exposed to different concentrations (10, 30 and 50 µg/mL) of chloroform and bromoform in vitro to analyse how these compounds affected the haematological count with increasing dose concentrations. Headspace gas chromatography analysis was also conducted on samples to assess the difference between measured and spiked values of doses. The results indicated that the damage caused by bromoform was statistically more significant as compared to chloroform. Haemoglobin (HGB) and mean corpuscular haemoglobin concentration levels lowered as they were significantly affected (p < 0.05) by bromoform at all administered doses. It also significantly damaged platelet level at doses of 30 (p < 0.05) and 50 µg/mL (p < 0.01). Conversely, the damage caused by chloroform was statistically less significant (p > 0.05).

Effect of metal ions and petrochemicals on bioremediation of chlorpyrifos in aerobic sequencing batch bioreactor (ASBR).

Application of chlorpyrifos (CP) has increased its environmental concentration. Increasing CP concentration has increased chances of adverse health effects. Its removal from environment has attained researcher's attention. CP degrading bacterial strains were isolated from wastewater and agricultural soil. Finally, selected five bacterial strains were identified using 16S rRNA nucleotide sequence analysis as Pseudomonas kilonensis SRK1, Serratia marcescens SRK2, Bacillus pumilus SRK4, Achromobacter xylosoxidans SRK5, and Klebsiella sp. T13. Interaction studies among bacterial strains demonstrated possibility for development of five membered bacterial consortium. Biodegradation potential of bacterial consortium was investigated in the presence of petrochemicals and trace metals. About 98 % CP removal was observed in sequencing batch reactors at inoculum level, 10 %; pH, 7; CP concentration, 400 mgL-1, and HRT, 48 h. Experimental data has shown an excellent fit to first order growth model. Among all petrochemicals only toluene (in low concentration) has stimulatory effect on biodegradation of CP. Addition of petrochemicals (benzene, toluene, and xylene) in high concentration (100 mg L-1) inhibited bacterial activity and decreased CP removal. At low concentration i.e., 1 mg L-1 of inorganic contaminants (Cu, Hg, and Zn) >96 % degradation was observed. Addition of Cu(II) in low concentration has stimulated CP removal efficiency. Hg(II) in all concentrations has strongly inhibited biodegradation rate except at 1 mgL-1. In simulated pesticide, wastewater CP removal efficiency decreased to 77.5 %. Outcomes of study showed that both type and concentration of petrochemicals and trace metals influenced biodegradation of CP.

Polyionic hybrid nano-engineered systems comprising alginate and chitosan for antihypertensive therapeutics.

Hydrophobic nature of virtually all antihypertensive (AHT) drugs is the major hindrance towards their oral administration. Current study focuses on the development of polyionic hybrid nano drug delivery systems comprising sodium alginate and chitosan, loaded with distinct AHT drugs (captopril, amlodipine and valsartan). Encapsulation efficiency of hybrid NCS increased in the order of amlodipine>valsartan>captopril with average value of 42±0.9%, 91±1.5% and 96±1.9%, respectively. Scanning electron microscopy revealed hybrid NCS with smooth topography and round appearance in case of captopril. FTIR analysis confirmed the cross-linking between amino and carboxylate group of chitosan and alginate to form polyionic structures at nano-scale. Zeta-sizer experiments revealed that particle size distribution had increased from 197±12nm to 341±15nm for void and captopril loaded NCS. However, highly positive zeta potential of +32±1.6mV was not decreased significantly. In vitro sustained release assays reflected excellent retention of AHT drug in hybrid nanoparticles at 4°C and 37°C in physiological buffer, as less than 8% of the total drug was released in first 24h. Thus, carbohydrate-based hybrid NCS offering high loading capacity, stability and sustained release of hydrophobic drugs can be excellent alternative to current AHT therapeutics.