Polysaccharides gums in drug delivery systems: A review.

For the drug delivery system, drug carriers' selection is critical to the drug's success in reaching the desired target. Drug carriers from natural biopolymers are preferred over synthetic materials due to their biocompatibility. The use of polysaccharide gums in the drug delivery system has received considerable attention in recent years. Polysaccharide gums are renewable resources and abundantly found in nature. They could be isolated from marine algae, microorganisms, and higher plants. In terms of carbohydrates, the gums are water-soluble, non-starch polysaccharides with high commercial value. Polysaccharide gums are widely used for controlled-release products, capsules, medicinal binders, wound healing agents, capsules, and tablet excipients. One of the essential applications of polysaccharide gum is drug delivery systems. The various kinds of polysaccharide gums obtained from different plants, marine algae, and microorganisms for the drug delivery system application are discussed comprehensively in this review paper.

Cellulose Nanocrystals (CNCs) and Its Modified Form from Durian Rind as Dexamethasone Carrier.

In this study, CNCs were extracted from durian rind. Modification to CNCs with saponin was conducted at 50 °C for one h. CNCs and CNCs-saponin were employed as dexamethasone carriers. Modification to CNCs using saponin did not change the relative crystallinity of CNCs. CNCs' molecular structure and surface chemistry did not alter significantly after modification. Both nanoparticles have surface charges independently of pH. Dexamethasone-released kinetics were studied at two different pH (7.4 and 5.8). Higuchi, Ritger-Peppas, first-order kinetic and sigmoidal equations were used to represent the released kinetic data. The sigmoidal equation was found to be superior to other models. The CNCs and CNCs-saponin showed burst release at 30 min. The study indicated that cell viability decreased by 30% after modification with saponin.

Low-cost structured alginate-immobilized bentonite beads designed for an effective removal of persistent antibiotics from aqueous solution.

The removal of persistent antibiotics from the water bodies can be quite challenging. The present study deals with the removal of doripenem, one of the most stable and persistent antibiotics, from aqueous solution via adsorption technique using the low-cost structured alginate-immobilized bentonite (Alg@iB) beads which can be easily recovered after the process. Alg@iB possesses a porous interior and higher basal spacing compared with the acid-activated bentonite (iB). Its adsorption/desorption isotherm corresponds to type IV IUPAC classification and H4-type hysteresis loops, implying the presence of slit- or plane-shaped pores. The influences of four independent adsorption parameters, e.g., pH, initial doripenem concentrations (md), temperature (T), and Alg@iB loading (mc), on the removal rate of doripenem (Yd) are investigated. The maximum Yd (95.8% w/w) is obtained at pH = 5, mc = 1.4% w/v, T = 50 °C, and md = 250 mg/l. The study suggests that the adsorption of doripenem is spontaneous and endothermic. Further analysis using the multi-linear intra-particle diffusion (IPD) model indicates that the rate-governing step in this adsorption process is the physical diffusion from the bulk solution to the boundary layer of Alg@iB. However, the mechanism study also considers the chemical hydrogen binding between the hydronium ions of Alg@iB and hydroxyl groups of doripenem as one of the driving forces that promote adsorption. Alg@iB shows good reusability with Yd > 90% w/w up to five adsorption cycles. Based on the study, the Alg@iB beads exhibit excellent affinity to doripenem, indicating that an effective doripenem removal can be achieved using this sorbent material.

Nanocelluloses: Sources, Pretreatment, Isolations, Modification, and Its Application as the Drug Carriers.

The 'Back-to-nature' concept has currently been adopted intensively in various industries, especially the pharmaceutical industry. In the past few decades, the overuse of synthetic chemicals has caused severe damage to the environment and ecosystem. One class of natural materials developed to substitute artificial chemicals in the pharmaceutical industries is the natural polymers, including cellulose and its derivatives. The development of nanocelluloses as nanocarriers in drug delivery systems has reached an advanced stage. Cellulose nanofiber (CNF), nanocrystal cellulose (NCC), and bacterial nanocellulose (BC) are the most common nanocellulose used as nanocarriers in drug delivery systems. Modification and functionalization using various processes and chemicals have been carried out to increase the adsorption and drug delivery performance of nanocellulose. Nanocellulose may be attached to the drug by physical interaction or chemical functionalization for covalent drug binding. Current development of nanocarrier formulations such as surfactant nanocellulose, ultra-lightweight porous materials, hydrogel, polyelectrolytes, and inorganic hybridizations has advanced to enable the construction of stimuli-responsive and specific recognition characteristics. Thus, an opportunity has emerged to develop a new generation of nanocellulose-based carriers that can modulate the drug conveyance for diverse drug characteristics. This review provides insights into selecting appropriate nanocellulose-based hybrid materials and the available modification routes to achieve satisfactory carrier performance and briefly discusses the essential criteria to achieve high-quality nanocellulose.

An environment-friendly composite as an adsorbent for removal Cu (II) ions.

The low-cost composite film was prepared by incorporating chitosan, berry soap fruit extract (rarasaponin), and bentonite as the raw materials. The produced chitosan/rarasaponin/bentonite (CRB) composite exhibits outstanding adsorption capability toward copper metal ions (Cu(II)). A series of static adsorption experiments were carried out to determine the isotherm and kinetic properties of CRB composite in the adsorption process. The adsorption equilibrium shows a good fit with the Langmuir isotherm model; the CRB composite has maximum uptake of Cu (II) of 412.70 mg/g; the kinetic adsorption data exhibit a good fit with the pseudo-second-order model. The thermodynamic parameters, ΔH°, ΔG°, and ΔS°, obtained from the isotherm data indicate that the uptake of copper ions by CRB composite is more favored at low temperatures. This study shows that physicochemical modified adsorbent, namely CRB composite, can remove Cu (II) better than pristine adsorbent of AAB and chitosan. The CRB composite also shows potential reusability.

Isolation and characterization of starch from Limnophila aromatica.

Starch is one of the digestible natural polymers found in vascular plants. This natural polymer is the primary source of polysaccharides to produce energy for humans. In this work, starch was extracted from the defatted and dephenolated Limnophila aromatica (DFPLA) by using the alkaline method. The DFPLA contains starch with a purity of 70.43 % where 55.1 % of it is the resistant starch. Physicochemical properties of the DFPLA starch such as solubility, morphology, swelling power, crystallinity, gelatinization, retrogradation, decomposition temperature, pasting profile, and surface functional groups were evaluated. The DFPLA starch possesses a medium-amylose content of 23.78 %, and the particle diameters of the starch were varied from 3 to 6 µm. The swelling power and solubility of the DFPLA starch are increasing as the temperature increased, where at 90 °C the swelling power and solubility of the starch is 13.73 g/g and 7.26%, respectively. Starch from DFPLA has a high total dietary fiber (76.28%) which is comparable to that of starch extracted from staple foods. The results indicate that starch from DFPLA possesses good physicochemical properties; this alternative starch may have potential application as a new feedstock for food industries.

Highly adsorptive chitosan/saponin-bentonite composite film for removal of methyl orange and Cr(VI).

Robust and simple composite films for the removal of methyl orange (MO) and Cr(VI) have been prepared by combining chitosan, saponin, and bentonite at a specific ratio. There are several composite films (chitosan-saponin-bentonite (CSB)) prepared; among them, the composite films CSB2:3 and CSB1:1 have the highest removal efficiency toward MO and Cr(VI) where the maximum removal is 70.4% (pH 4.80) and 92.3% (pH 5.30), respectively. It was found that different types of adsorbate have different thermodynamic properties of the adsorption process; the adsorption of MO onto CSB2:3, chitosan, and acid-activated bentonite (AAB) proceeded endothermically, while the adsorption of Cr(VI) onto CSB1:1, chitosan, and AAB proceeded exothermically. The parameters of the adsorption were modeled by using isotherm and kinetic equations. The models of Langmuir, Freundlich, Redlich-Peterson, Sips, and Toth were used for fitting the adsorption isotherm data at a temperature of 30, 45, and 60 °C; all of the isotherm models could represent the data well. The result indicates that CSB2:3 has the highest adsorption capacity toward MO with qm of 360.90 mg g-1 at 60 °C; meanwhile, CSB1:1 has the highest adsorption capacity toward Cr(VI) with qm 641.99 mg g-1 at 30 °C. The pseudo-second-order model could represent the adsorption kinetics data better than the pseudo-first-order equation. The adsorption mechanism was proposed, and the thermodynamic properties of the adsorption were also studied.

Rarasaponin-bentonite-activated biochar from durian shells composite for removal of crystal violet and Cr(VI) from aqueous solution.

This paper presents the preparation of composite material and its application for the adsorption of crystal violet and Cr(VI) from aqueous solution onto acid-activated bentonite (AAB) and rarasaponin-bentonite-activated biochar from durian shells composite (RBAB). The influence of initial pH of the solution and the temperature of adsorption on the adsorbents adsorption performance was also studied. Langmuir and Freundlich models could represent the adsorption equilibria equally well. Thermodynamic parameters such as ∆G°, ∆H°, and ∆S° were evaluated based on the adsorption isotherms. The values of ∆G°, ∆H°, and ∆S° for crystal violet adsorption system demonstrate behavior contrary to the Cr(VI) adsorption system. Where crystal violet adsorption is preferred at high temperatures with qmax, value is 518.64 mg/L; while adsorption Cr(VI) is better at low temperature with qmax, value is 106.30 mg/L. Pseudo-first-order and pseudo-second-order kinetic models could represent the kinetic data well.

Adsorption and photocatalytic performance of bentonite-titanium dioxide composites for methylene blue and rhodamine B decoloration.

Bentonite - TiO2 composites were prepared by impregnation of TiO2 and bentonite, followed by microwave irradiation processes. The composites were characterized using FTIR, SEM, XRD, and nitrogen sorption methods. Anatase phase of TiO2 in all composites are observed through XRD diffraction peaks and surface morphology of the composites. The adsorption and photocatalytic capabilities of the composites were tested in liquid phase adsorption of methylene blue and Rhodamine B. The adsorption and photocatalytic degradation experiments were conducted in the presence or absence of UV light irradiation. Langmuir and Freundlich models were employed to correlate the experimental adsorption data, and it was found that Langmuir gave better performance in correlating the experimental data. Modification of Langmuir equation to accommodate photocatalytic degradation process was conducted, and the model could represent the experimental results very well.