Microalgae to bioenergy production: Recent advances, influencing parameters, utilization of wastewater - A critical review.

Fossil fuel limitations and their influence on climate change through atmospheric greenhouse gas emissions have made the excessive use of fossil fuels widely recognized as unsustainable. The high lipid content, carbon-neutral nature and potential as a biofuel source have made microalgae a subject of global study. Microalgae are a promising supply of biomass for third-generation biofuels production since they are renewable. They have the potential to produce significant amounts of biofuel and are considered a sustainable alternative to non-renewable energy sources. Microalgae are currently incapable to synthesize algal biofuel on an extensive basis in a sustainable manner, despite their significance in the global production of biofuels. Wastewater contains nutrients (both organic and inorganic) which is essential for the development of microalgae. Microalgae and wastewater can be combined to remediate waste effectively. Wastewater of various kinds such as industrial, agricultural, domestic, and municipal can be used as a substrate for microalgal growth. This process helps reduce carbon dioxide emissions and makes the production of biofuels more cost-effective. This critical review provides a detailed analysis of the utilization of wastewater as a growth medium for microalgal - biofuel production. The review also highlights potential future strategies to improve the commercial production of biofuels from microalgae.

Study the anticancer efficacy of doxorubicin-loaded redox-responsive chitosan-derived nanoparticles in the MDA-MB-231 cell line.

This study focuses on the design and evaluation of redox-responsive nanoparticles (NPs) by synthesizing disulfide-containing N-phthaloyl chitosan-SS-methoxy poly(ethylene glycol) (NPC-SS-mPEG) and incorporating the anti-cancer drug doxorubicin into the NPs. The structural features of NPC-SS-mPEG were investigated using FTIR, NMR, XRD, and TGA/DTA analysis. DLS and TEM analysis confirmed the particle size and morphology of the NPs. The stability of the NPs was measured with the presence and absence of glutathione (GSH) in buffers pH 5 and 7.4. Furthermore, the release of DOX from the NPs was studied in GSH (10 mM) containing/absent medium at pH 5 and pH 7.4 which mimics the intracellular environment with redox potential. The results indicated a significantly increased release of DOX in the GSH containing medium pH 5 (82.9 ± 2.1 %) and pH 7.4 (67.37 ± 0.88 %) compared to the GSH free pH 7.4 (29.99 ± 1.01 %) and pH 5 medium (56.56 ± 1.7 %) at 60 h. The cytotoxicity study in the MDA-MB-231 breast cancer cell line by MTT assay indicated higher toxicity of redox-responsive NPs to cancer cells than free DOX. In concurrence with the cytotoxicity assay, in-vitro fluorescence staining assays (AO/EB, Hoechst, ROS generation) also confirmed that NPs loaded with DOX induce higher toxicity to cancer cells than free DOX. Taken together, the overall results confirmed the superiority of the redox response-mediated release of DOX in effectively controlling cancer progression.