Cancer is one of the most common lethal diseases and the leading cause of mortality worldwide. Effective cancer treatment is a global problem, and subsequent advancements in nanomedicine are useful as substitute management for anti-cancer agents. Nanotechnology, which is gaining popularity, enables fast-expanding delivery methods in science for curing diseases in a site-specific approach, utilizing natural bioactive substances because several studies have established that natural plant-based bioactive compounds can improve the effectiveness of chemotherapy. Bioactive, in combination with nanotechnology, is an exceptionally alluring and recent development in the fight against cancer. Along with their nutritional advantages, natural bioactive chemicals may be used as chemotherapeutic medications to manage cancer. Alginate, starch, xanthan gum, pectin, guar gum, hyaluronic acid, gelatin, albumin, collagen, cellulose, chitosan, and other biopolymers have been employed successfully in the delivery of medicinal products to particular sites. Due to their biodegradability, natural polymeric nanobiocomposites have garnered much interest in developing novel anti-cancer drug delivery methods. There are several techniques to create biopolymer-based nanoparticle systems. However, these systems must be created in an affordable and environmentally sustainable way to be more readily available, selective, and less hazardous to increase treatment effectiveness. Thus, an extensive comprehension of the various facets and recent developments in natural polymeric nanobiocomposites utilized to deliver anti-cancer drugs is imperative. The present article provides an overview of the latest research and developments in natural polymeric nanobiocomposites, particularly emphasizing their applications in the controlled and targeted delivery of anti-cancer drugs.

Interpenetrating network (IPN) beads of sodium carboxymethyl cellulose (SCMC) and sodium carboxymethyl xanthan (SCMX) containing diclofenac sodium (DS), a non steroidal anti-inflammatory drug were prepared by single water-in-water (w/w) emulsion gelation process using AlCl₃ as the cross-linking agent. The influence of different formulation variables like polymer ratio, gelation time, concentration of cross-linking agenton in-vitro physico-chemical parameters and drug release studies were performed. The tailored IPN bead were analytically evaluated by Scanning electron microscopy (SEM), Fourier Transform Infra-red (FTIR), X-ray diffraction (XRD), Differential Scanning Calorimetry (DSC) analysis. IPN beads showed improved drug encapsulation efficiency along with enhanced intestinal drug release.

Polymers that bear reversible massive, physical or chemical changes in response to little peripheral changes within the environmental conditions are Smart polymers, having versatility and tunable sensitivity. They have very promising applications in the biomedical field. This study will delve into the underlying principles along with entire features of these sensitive polymers and their most current and relevant applications to solve biological problems.

Objective. The objective of this work encompasses the application of the response surface approach in the development of buccoadhesive pharmaceutical wafers of Loratadine (LOR).Methods. Experiments were performed according to a 3²factorial design to evaluate the effects of buccoadhesive polymer, sodium alginate (A), and lactose monohydrate as ingredient, of hydrophilic matrix former (B) on the bioadhesive force, disintegration time, percent (%) swelling index, and time taken for 70% drug release (t70%). The effect of the two independent variables on the response variables was studied by response surface plots and contour plots generated by the Design-Expert software. The desirability function was used to optimize the response variables.Results. The compatibility between LOR and the wafer excipients was confirmed by differential scanning calorimetry, FTIR spectroscopy, and X-ray diffraction (XRD) analysis. Bioadhesion force, measured with TAXT2i texture analyzer, showed that the wafers had a good bioadhesive property which could be advantageous for retaining the drug into the buccal cavity.Conclusion. The observed responses taken were in agreement with the experimental values, and Loratadine wafers were produced with less experimental trials, and a patient compliant product was achieved with the concept of formulation by design.

Purpose. The objective of the proposed work is to evaluate the efficacy of Pectins to qualify them as polymers for designing an oral microsphere for the delivery of selected oral antidiabetic drug-like metformin hydrochloride. Methods. Different Microspheres formulations were prepared by the water in oil (w\o) emulsion solvent evaporation technique and subsequently evaluated for its different physical parameters as well as its in vitro and in vivo drug release study. Results. The formulations F2 (98.42) and F3 (98.03) showed a constant and high release in the dissolution profile, so among these two formulations, F2 was taken for development study, due to the better result shown over in other evaluation parameters. From the HPLC determinations after in vivo study, it had been found that the test samples and the standard sample had not shown any significant fluctuation in relation to their retention time. Conclusion. From in vitro and in  vivo results, it may be concluded that drug-loaded pectin microspheres in 1 : 1 ratio are a suitable delivery system for metformin hydrochloride and may be used for effective management of NIDDM. From this experiment, it could be concluded that as a natural polymer, pectin has potentiality in novel drug delivery system.

The purpose of this research is to investigate the effect of addition of surfactant and water in diesel and to make an emulsified fuel considering the needs for vehicle performance and its cleanest possible operation. The total surfactant concentration in each of the diesel-water emulsion samples studied (span 20, span 80, tween 20, tween 80) is fixed at 1% w/w. The water content is variable at 5–15% w/w and the diesel content is varied from 84 to 94% w/w. Among all the tested nonionic surfactants, tween 80 is found to prominently reduce the carbon monoxide (CO), hydrocarbon (HC), and nitrogen oxide (NOx) emissions. Tween 20 reduced the NOx emission to a greater extent. Diesel emulsion with a fixed ratio of span 80 and tween 80 (1:1) efficiently reduced the overall emissions as compared to diesel alone. The developed diesel emulsion employed with nonionic surfactants clearly reduced the harmful engine emissions such as CO, HC, and NOx, signifying them as a future potential emulsifier in diesel fuel emulsion.