Formulating a novel drilling mud using bio-polymers, nanoparticles, and SDS and investigating its rheological behavior, interfacial tension, and formation damage.

Formation damage is a well-known problem that occurs during the exploration and production phases of the upstream sector of the oil and gas industry. This study aimed to develop a new drilling mud formulation by utilizing eco-friendly bio-polymers, specifically Carboxymethyl Cellulose (CMC), along with nanostructured materials and a common surfactant, sodium dodecyl sulfate (SDS). The rheological properties of the drilling fluid and the impact of additives on its properties were investigated at the micromodel scale, using a flow rate of 20 mL/h. The polymer concentration and nano clay concentration were set at two levels: 0.5 wt% and 1 wt%, respectively, while the surfactant content was varied at three levels: 0.1 wt%, 0.4 wt%, and 0.8 wt%. The results of the interfacial tension (IFT) analysis demonstrated a significant decrease in the interfacial tension between oil and water with the increasing concentration of SDS. Furthermore, following the API standard, the rheological behavior of the drilling fluid, including the gel strength and thixotropic properties of the mud, was evaluated with respect to temperature changes, as this is crucial for ensuring the inherent rheological stability of the mud. The rheological analysis indicated that the viscosity of the mud formulation with nanoparticles experienced a reduction of up to 10 times with increasing shear rate, while other formulations exhibited a decline of 100 times. Notably, the rheological properties of the Agar specimen improved at 150 °F due to its complete solubility in water, whereas other formulations exhibited a greater drop in viscosity at this temperature. As the temperature increased, drilling fluid containing nanostructured materials exhibited higher viscosity.

Targeted Delivery of Anticancer Drug Loaded Charged PLGA Polymeric Nanoparticles Using Electrostatic Field.

Pure positive electrostatic charges (PPECs) show suppressive effect on the proliferation and metabolism of invasive cancer cells without affecting normal tissues. PPECs are used for the delivery of drug-loaded polymeric nanoparticles (DLNs) capped with negatively charged poly(lactide-co-glycolide) (PLGA) and Poly(vinyl-alcohol) PVA into the tumor site of mouse models. The charged patch is installed on top of the skin in the mouse models' tumor region, and the controlled selective release of the drug is assayed by biochemical, radiological, and histological experiments on both tumorized models and normal rats' livers. It is found that DLNs synthesized by PLGA show great attraction to PPECs due to their stable negative charges, which would not degrade immediately in blood. The burst and drug release after less than 48h of this synthesized DLNs are 10% and 50%, respectively. These compounds can deliver the loaded-drug into the tumor site with the assistance of PPECs, and the targeted-retarded release will take place. Hence, local therapy can be achieved with much lower drug concentration (conventional chemotherapy [2 mg kg-1 ] versus DLNs-based chemotherapy [0.75 mg kg-1 ]) with negligible side effects in non-targeted organs. PPECs have many potential clinical applications for advanced-targeted chemotherapy with the lowest discernible side effects.

Reinforced Poly(ε-caprolactone) Bimodal Foams via Phospho-Calcified Cellulose Nanowhisker for Osteogenic Differentiation of Human Mesenchymal Stem Cells.

In this work, phospho-calcified cellulose nanowhiskers (PCCNWs) were prepared from wastepaper powder (WPP) and were dispersed in poly(ε-caprolactone) (PCL). The biocompatible and biodegradable (PCL)/PCCNW bimodal foam nanocomposites with two species cell sizes were prepared by the solvent casting/particulate leaching method in different weight percentage of PCCNWs. The mechanical, thermal, and in vitro biological properties of PCL/PCCNW nanocomposites were investigated. All PCL/PCCNW scaffolds were hydrophilic, biodegradable, and also noncytotoxic. The human mesenchymal stem cells were cultured on the prepared PCL/PCCNW bimodal foam nanocomposites and differentiated to osteoblasts. On the basis of evaluating tests such as MTT assay, acridine orange/ethidium bromide staining, alkaline phosphatase assay, calcium content assay, and alizarin red staining, PCL/PCCNW scaffolds were introduced as an appropriate option for emulating the behavior of extracellular matrix. Increasing PCCNWs improves the mechanical, hydrophilic, and biodegradability properties of the nanocomposites as well as their osteoconductivity.

Poly(ε-caprolactone)/triclosan loaded polylactic acid nanoparticles composite: A long-term antibacterial bionanocomposite with sustained release.

In this study, the antibacterial bionanocomposites of poly(ε-caprolactone) (PCL) with different concentrations of triclosan (TC) loaded polylactic acid (PLA) nanoparticles (30wt% triclosan) (LATC30) were fabricated via a melt mixing process in order to lower the burst release of PCL and to extend the antibacterial activity during its performance. Due to the PLA's higher glass transition temperature (Tg) and less flexibility compared with PCL; the PLA nanoparticles efficiently trapped the TC particles, reduced the burst release of TC from the bionanocomposites; and extended the antibacterial property of the samples up to two years. The melt mixing temperature was adjusted to a temperature lower than the melting point of LATC30 nanoparticles; therefore, these nanoparticles were dispersed in the PCL matrix without any chemical reaction and/or drug extraction. The sustained release behavior of TC from PCL remained unchanged since no significant changes occurred in the samples' crystallinity compared with that in the neat PCL. The elastic moduli of samples were enhanced once LATC30 is included. This is necessary since the elastic modulus is decreased with water absorption. The rheological behaviors of samples showed appropriate properties for melt electro-spinning. A stable process was established as the relaxation time of the bionanocomposites was increased. The hydrophilic properties of samples were increased with increasing LATC30. The proliferation rate of the fibroblast (L929) cells was enhanced as the content of nanoparticles was increased. A system similar to this could be implemented to prepare long-term antibacterial and drug delivery systems based on PCL and various low molecular weight drugs. The prepared bionanocomposites are considered as candidates for the soft connective tissue engineering and long-term drug delivery.

Effect of hydroxyapatite nano-particles on morphology, rheology and thermal behavior of poly(caprolactone)/chitosan blends.

The effect of hydroxyapatite nano-particles (nHA) on morphology, and rheological and thermal properties of PCL/chitosan blends was investigated. The tendency of nHA to reside in the submicron-dispersed chitosan phase is determined using SEM and AFM images. The presence of electrostatic interaction between amide sites of chitosan and ionic groups on the nHA surface was proved by FTIR. It is shown that the chitosan phase is thermodynamically more favorable for the nano-particles to reside than the PCL phase. Lack of implementation of Cox-Merz theory for this system shows that the polymer-nano-particle network is destructed by the flow. Results from dynamic rheological measurements and Zener fractional model show that the presence of nHA increases the shear moduli and relaxation time of the PCL/chitosan blends. DSC measurements showed that nHA nano-particles are responsible for the increase in melting and crystallization characteristics of the PCL/chitosan blends. Based on thermogravimetric analysis, the PCL/chitosan/nHA nano-composites exhibited a greater thermal stability compared to the nHA-free blends.

Investigating composite systems based on poly L-lactide and poly L-lactide/triclosan nanoparticles for tissue engineering and medical applications.

In this study, the encapsulated triclosan with a low molecular weight PLLA (LATC30) is dispersed into a PLLA having higher molecular weight via melt blending to increase the overall properties and particularly antibacterial activity of the system. The proposed method results in a completely homogenous composite as 5% LATC30 improved mechanical properties. For instance, the elongation at break was increased ca. 3%. The mechanical properties of the fabricated composites were also affected by the plasticizing role of LATC30. The kinetics of hydrolytic degradation in an accelerated condition was obtained using a novel method by the Beer-Lambert equation. It was found that the incorporation of LATC30 into the composite increases the rate of hydrolytic degradation. The calorimetry showed a reduction in crystallinity upon addition of LATC30. Moreover, the degradation of the composites was studied and fully described the kinetic analysis by the Flynn-Wall-Ozawa (FWO) method. From which, it was found that the activation energy of the system was decreased. As the LATC30 content of the composite was increased, the hydrophilicity of the composite was increased. The fabricated scaffolds with 5% LATC30 demonstrated a good osteoblast cell attachment and mineralization on the composite scaffolds. This composite is a suitable antibacterial candidate for the bone tissue engineering and medical applications since the real dosage of triclosan stays at ca. 1.5%.

PCL/chitosan/Zn-doped nHA electrospun nanocomposite scaffold promotes adipose derived stem cells adhesion and proliferation.

Chitosan (Ch), and poly(ɛ-caprolactone) (PCL), widely used as biomaterials with desirable properties for tissue engineering applications, were both blended with zinc-doped hydroxyapatite nanoparticles(nZnHA) and electrospun into nanofibrous scaffolds using formic acid/acetic acid. The rationale behind this study was to demonstrate that presence of small quantities of Zn(2+) ions doped in HA nanoparticles can improve biocompatibility of PCL/Ch blends. SEM observation revealed that average fiber diameter was increased from about 136 nm for a PCL/Ch blend, to around 210 nm for PCL/Ch/nZnHA nanocomposite. PCL/Ch/nZnHA scaffolds offered higher elastic modulus (about 3-fold) and tensile strength (nearly 1.5-fold) than the corresponding PCL/Ch scaffolds. In-vitro biocompatibility studies using human adipose derived stem cells (hAD-MSCs), demonstrated that the presence of only 5 wt% nZnHA in PCL/Ch/nZnHA nanocomposites enhanced hAD-MSCs' attachment compared to PCL/Ch and PCL/Ch/nHA. Finally, hAD-MSCs proliferation occurred at significantly higher rates of 1.5, 1.3 and 1.2 times on PCL/Ch/nZnHA scaffold compared to PCL, PCL/Ch and PCL/Ch/nHA, respectively.

Evaluation of melt rheology of lactose-filled polyethylene glycol composites by means of capillary rheometery.

In this study melt rheological behavior of lactose-filled polyethylene glycol (PEG) composites as a low melting polymeric carrier for controlled release drugs was investigated using a capillary rheometer. The effect of lactose concentration and process variables such as temperature and ram speed on the flow behavior of PEG has been studied. The composites were found to be shear thinning in behavior when extruded, and the results were well described by power-law model in each case. Stronger shear thinning behavior was observed by raising the filler concentration and decreasing the temperature, while the flow index has been decreased. In all compositions a significant increase in shear viscosity was found by an increase in the filler content. In fact, shear viscosity increased linearly by weight fraction of filler, but there was a dramatic increase after the filler content raised above 20 wt% of lactose which might be the result of the strong interaction among filler particles. Furthermore, decreasing the process temperature resulted in an increase in shear viscosity, and the temperature dependence of shear viscosity decreased as the shear rate increased. The extensional viscosity of composites was calculated in each case. The results showed that the ratio of the extensional viscosity to shear viscosity was in the range of 500-1200.

Rheological evaluation of wet masses for the preparation of pharmaceutical pellets by capillary and rotational rheometers.

The rheological properties of wet powder masses used in the preparation of pharmaceutical pellets by extrusion/spheronization were evaluated utilizing capillary and rotational rheometers. A ram extruder was used as a capillary rheometer to construct flow and viscosity curves for each wet mass under different extrusion rates and die geometry. As a result, shear thinning behavior was observed for all wet masses. Among the considered rheological models Power Law and Herschel-Bulkley models fitted well with the experimental results. For the majority of the wet masses, water separation and migration occurred during extrusion which led to uneven water content in the extrudate. The effect of extrusion condition including extrusion speed, die geometry and water content on the occurrence of water separation was investigated and the surface quality of the extrudates was compared. In addition, dynamic rheometry tests were done by a parallel plate rheometer to investigate the viscoelastic properties of the wet masses. The frequency sweep tests showed that as water content of the wet masses decreases storage (G') and loss modulus (G″) increase. The storage modulus values were much higher than those of the loss modulus showing dominated elastic rather than viscous behavior for the wet masses at low deformation rates.