Dissolution Percentage Research Articles

Comparison of In-Vitro Dissolution of Griseofulvin Tablet made from Nano Particles and Solid Dispersion

Objectives: To find out the comparison of dissolution results of griseofulvin tablets made from nanoparticles, solid dispersions, and conventional materials.
 Interventions: Different types of active ingredients in the form of nanoparticles and solid dispersions can affect the dissolution results of tablets.
 Main outcomes measure: The results obtained in this study are the cumulative dissolution percentage and the order kinetics of the release of active ingredients.
 Conclusion: There was no significant cumulative percent drug release difference (p> 0.05) between nano particles, solid dispersions, and conventional materials. Tablets containing active nanoparticles, solid dispersions, and conventional materials show a linear relationship with a correlation coefficient (R2) close to 1, shown in zero-order kinetics models.
 

Effect of ground wood particle size on biomass fractionation using p-toluenesulfonic acid treatment

Size reduction of biomass is an energy-extensive operation for biorefinery, and fundamentals of size effect on biomass fractionation is pressing to be unraveled. Herein, we investigated effect of ground wood particle size on properties of biomass fractionation using p-toluenesulfonic acid (p-TsOH) treatment. Both carbohydrates and lignin dissolution increased with smaller ground wood particle size. Comparatively, delignification performance was much affected by ground wood particle size, and the percentage of lignin dissolution was dramatically enhanced at small ground wood particle size. The excellent delignification selectivity was warranted at small ground wood particle size accordingly. In addition, mechanism of ground wood particle size effect on lignin dissolution was proposed. On one hand, dissolution of lignin by p-TsOH primarily was an aggregation effect, and diffusion of lignin from the microfibril network in biomass became growingly troublesome at large size. On the other hand, depolymerization of lignin mainly occurred in the liquid phase, which essentially led to production of large p-TsOH-lignin aggregates with low diffusivity.

EVALUATION OF INNOVATED FORMULA OF BISACODYL SUPPOSITORY FOLLOWING THE DISSOLUTION PROFILE AND STABILITY DATA USING DEVELOPED HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHOD

Objective: Bisacodyl is a laxative drug used in the treatment of constipation, it is soluble in mineral acids, but it is practically insoluble in water. Therefore, it is very hard task to dissolve bisacodyl in alkaline medium so the objective of this study was the development of proper dissolution method for a new formulation of bisacodyl suppositories in a medium simulated to rectal region. Obviously, most of the bisacodyl suppositories preparation products will yield low percentages of dissolution in the alkaline medium of phosphate buffer pH 7.2.
 Methods: Preparation inclusion complex of bisacodyl with the solubilizing agent beta-cyclodextrin then incorporated in a suppository base. The quantitative analysis of bisacodyl in suppositories was carried by a developed and validated high-performance liquid chromatography method.
 Results and Discussion: The dissolution rates for the innovated formulation of bisacodyl complexed with beta-cyclodextrin suppositories were in average of 97.5% and the stored suppositories of this formulation maintained their specified physical and chemical properties along the real stability study.
 Conclusion: The application of the inclusion complexation technique of bisacodyl with beta-cyclodextrin in the production of suppositories enhances the dissolution rate and improves the stability of suppositories performance.

Pressure Sulfuric Acid Leaching of Manganese-Rich Slag with Pyrite as Additive

Large amounts of manganese-rich slag were generated from smelting low-grade manganese ore containing high iron and high phosphorus in electric furnace or blast furnace, which contain 25–40 mass% Mn. This paper describes an efficient hydrometallurgical process for the utilization of high manganese slag instead of conventional usage of pyrometallurgical route for manganese recovery. Pressure acid leaching of manganese-rich slag using air as pressurized gas is studied systematically. The effects of mass ratio of manganese-rich slag to pyrite, concentration of sulfuric acid, leaching temperature, partial air pressure, leaching time, and liquid-solid (L/S) ratio on the separation of manganese with other main impurity components were investigated comprehensively. Under the following optimal process conditions, weight of manganese-rich slag powder,100 g; mass ratio of manganese-rich slag to pyrite, 20:1; sulfuric acid concentration of 140 g/L; air pressure of 0.6 MPa; leaching temperature of 140 °C; leaching time of 1 h; L/S of 7:1; ore size of 75–80 μm; and stirring rate of 600 rpm, the extraction rate of Mn reached 94%, and the dissolution percentage of Si, Al, and Fe are as low as 2%, 6%, and 10%, respectively. The leaching slurry presented a good solid-liquid separation characteristic. The silicic acid formed during sulfuric acid leaching manganese silicates was converted to filterable dehydrated SiO2 particles which precipitated in the residue under the condition of higher temperature with higher pressure. The effect of adding pyrite may be to reduced iron ions and decreased the output of iron hydroxide colloid and also reduced MnO2 to manganese sulfate in sulfuric acid leaching. Thus the formation possibility of colloid such as silica gel and iron hydroxide was decreased, and higher yield of manganese sulfate could be achieved.

Optimization and Modeling of Leaching Parameters Affecting Nickel Dissolution from Lateritic Ore in Eskisehir (Mihaliccik-Yunusemre) Using Box-Behnken Experimental Design

In this study, optimization and modeling of leaching parameters affecting nickel dissolution from lateritic ore in EskiAƒâ€¦A‚A¸ehir (MihalAƒâ€žA‚±ccAƒâ€žA‚±k-Yunusemre) were investigated using Box-Behnken design. Stirring speed (100-400 rpm, temperature (40-80°C), acid concentration (0.1-2 M) and dissolution time (30-180 min) were selected as experimental design parameters. 27 experiments were carried out by Box-Behnken experimental design in Minitab 16.0 program. After leaching experiments, the highest Ni dissolution percentages were obtained as 87.85%. The effective parameters and their interactions in nickel dissolution are described with a mathematical model. The results obtained from the experiments were subjected to ANOVA and multiple regression analysis. The R2 value of the model for nickel dissolution was calculated as 0.980. This showed that the predicted values are in good agreement with the observed values. In addition, three-dimensional response surface and contour graphs of the parameters affecting nickel dissolution efficiency were created and the results were examined.

Physicochemical Evaluation of Brands of Amlodipine Besylate Tablets.

Background: Hypertension is a chronic condition, and the cost of filling prescriptions has a potential of putting a financial strain on patients, hence the need for lower priced but bioequivalent generics. The Nigerian drug market is awash with generics of Amlodipine besylate, a first line drug in the treatment of hypertension, therefore, any prescribed alternative must be bioequivalent to the originator. Objectives: This study assessed the physicochemical properties of some brands in order to predict pharmaceutical and bioequivalence and invariably, the interchangeability with the innovator brand. Methods: Compendial parameters of average weight, friability, disintegration, drug content and dissolution profile of ten generic brands were evaluated using the United States Pharmacopeia (USP) as well as the non-official hardness test. Results: Two brands failed the test for hardness, while still keeping to the stipulated friability limit. All the brands met the required disintegration time, irrespective of the discordance of some brands in the breaking force and friability values. All brands were found to contain between 92.00 and 103.57% (w/w) of Amlodipine besylate. Two brands failed to achieve ≥75% dissolution expected at 30 minutes and this was reflected in the low f2 values of 35.06% and 28.73%. The dissolution curves displayed a similarity for two brands, which was also corroborated by the high percentage dissolution efficiency (DE) of 92.00%, as well as the f1 and f2 values, compared to the innovator brand. Conclusion: Although the parameters used may predict therapeutic equivalence, interchangeability with the comparator brand is subject to relevant bioequivalence studies.

In-Vitro Evaluation of Anti-Urolithic Activity of Leaves Extract of Costus igneus

Recent advances in drug therapy has tremendously increased due to its demand with the ever growing health care needs. Occurrence of many dreadful diseases including liver, kidney, heart disorders are now a day's very common and people prefer modern medicines as compare to conventional medicines. But Scientific knowledge and exploration and technological advancements had made plant derived medicine as a choice of therapy in many ailments. Many novel and safe herbal preparations are effectively used in treatment. Urolithiasis is common condition of development of calculi or stone in urinary system specially ureter and gall bladder. Many Herbal formulations like neeri, cystone etc. are widely available in the market and has proven potential in the management of disease. In the present investigation methanolic extract of leaves of Costus igneus was used to analyse its In-vitro anti-urolithic activity. The percentage dissolution of calcium oxalate in the presence of extract in semipermeable egg membrane was studied and compared with standard drug cystone. The percentage dissolution of methanolic extract and standard drug cystone was found to be 86.12% and 80.34% respectively. The results suggests that the plant can be used for the effective treatment of urolithiasis and can be added in the preparation of polyherbal formulation.

Particle engineering of fenofibrate for advanced drug delivery system

BackgroundThe goal of the current investigation was to formulate, evaluate co-crystal, and further design of solid unit dosage form of antihyperlipidemic BCS class II drug fenofibrate (FNO). Co-crystals composed of a structurally homogeneous crystalline material that contains two or more components in a definite stoichiometric amount helps in increasing yield, the capability to regulator polymorph fabrication, enhanced invention crystallinity. Ball milling method is used for co-crystal formulation, optimized via 32 full factorial design and characterized by saturation solubility, particle size analysis, Fourier transform infrared spectroscopy (FT-IR) study analysis, powder X-ray diffraction (PXRD) study analysis, surface morphology by scanning electron microscopy (SEM) study, flow properties, and ex vivo intestinal permeation study via non-everted rat intestinal sac model. Furthermore, optimized batch compressed into tablets is evaluated for disintegration time, hardness, friability, in vitro drug release study and stability study.ResultsIt demonstrated that co-crystal formulation FNOCC7 shows higher saturation solubility 0.3874 ± 2.82 g/ml with less particle size 221.231 ± 0.456 nm, FT-IR spectra confirmed significant structural alterations in the formulation indicating the hetero-molecular interaction, the presence of hydrogen bonding had occurred in the co-crystals, PXRD spectra of formulation determined by the increase in the crystalline nature. FNO co-crystals show flux (F) and permeability coefficient (Papp) 0.322 ± 0.068 μg/min, 5.38 ± 0.093 cm/min respectively increased compared to the pure drug makes in an enhancement of solubility as well as the bioavailability of BCS class II drug.ConclusionsThe solubility and dissolution percentage of FNO can be improved by the utilization of Co-crystal of FNO with PEG 4000. The solubilization impact of PEG 4000 might be contributed because of the decrease of molecule conglomeration of the drug presence of crystallinity, expanded wettability, and dispersibility; pharmaceutical co-crystals speak to a beneficial class of crystal form with regard of pharmaceuticals.

Chemical dissolution of iron substituted chromium oxide by dissolved ozone

Dissolved Ozone based formulations are regarded as good chemical decontamination reagents for the chromium oxide covered alloy surfaces. The present article highlights the optimization of process parameters for the dissolved ozone based process. The parameters like solution pH and temperature, input ozone and iron content in oxide on the dissolution behavior of the chromium oxide were studied. Presence of carbonate/bicarbonate in the dissolved ozone increases the dissolution of chromium oxide. Addition of 5 and 10 mM carbonate showed increase in the percentage dissolution by 1.6 and 2.9 times at fixed input of ozone compared to the absence of carbonate. Presence of iron in the chromium oxide lattice lowers the oxide dissolution in dissolved ozone medium. Lowering the pH helps in release of iron from the oxide lattice enabling a higher percentage of oxide dissolution.

Preparation of ursolic acid–phospholipid complex by solvent-assisted grinding method to improve dissolution and oral bioavailability

To improve the aqueous solubility and the oral bioavailability of a poorly water-soluble biologically active pentacyclic triterpenoid, ursolic acid (UA), ursolic acid–phospholipid complex (UA–PC) was prepared using solvent-assisted grinding method which is green and simple. The phospholipid complex was characterized by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), scanning electron microscope (SEM), and transmission electron microscope (TEM), which confirmed the formation of the phospholipid complex. Specifically, compared with free UA, the formulation demonstrated over 276-fold higher aqueous solubility of UA and exhibited faster dissolution rate and higher cumulative dissolution percentages. Finally, the oral bioavailability of the prepared UA–PC was evaluated using Sprague-Dawley (SD) rats. Compared with free UA, the UA–PC exhibited considerable enhancement in the bioavailability with an increase in Cmax (183.80 vs 68.26 μg/l) and AUC 0–24 h (878.0 vs 212.1 μg·h/l), which was consistent with the in vitro results. This enhancement was attributed to the improvement of solubility and dissolution in vitro. Therefore, the method of solvent-assisted grinding appears to be an efficient approach for the preparation of UA–PC, and the prepared UA–PC showed a promising potential to overcome the limitation of poor oral bioavailability associated with low water solubility.

Delineating the effects of hot-melt extrusion on the performance of a polymeric film using artificial neural networks and an evolutionary algorithm.

The aim of this study was to utilize an artificial neural network (ANN) in conjunction with an evolutionary algorithm to investigate the relationship between hot melt extrusion (HME) process parameters and vaginal film performance. Investigated HME process parameters were: barrel temperature, screw speed, and feed rate. Investigated film performance attributes were: percent dissolution at 30min, puncture strength, and drug content. An ANN model was successfully developed and validated with a root mean squared error of 0.043 and 0.098 for training and validation, respectively. Of all three assessed process parameters, the model revealed that barrel temperature has a significant impact on film performance. An increase in barrel temperature resulted in increased dissolution and punctures strength and decreased drug content. Additionally, a successful implementation of an evolutionary algorithm was carried out in order to demonstrate the potential applicability of the developed ANN model in film formulation optimization. In this analysis, the values predicted of film performance attributes were within 1% error of the experimental data. The findings of this study provide a quantitative framework to understand the relationship between HME parameters and film performance. This quantitative framework has the potential to be used for film formulation development and optimization.

Effects of long-term exposure to reduced pH conditions on the shell and survival of an intertidal gastropod

Volcanic CO2 vents are useful environments for investigating the biological responses of marine organisms to changing ocean conditions (Ocean acidification, OA). Marine shelled molluscs are highly sensitive to changes in seawater carbonate chemistry. In this study, we investigated the effects of reduced pH on the intertidal gastropod, Phorcus sauciatus, in a volcanic CO2 vent off La Palma Island (Canary Islands, North East Atlantic Ocean), a location with a natural pH gradient ranging from 7.0 to 8.2 over the tidal cycles. Density and size-frequency distribution, shell morphology, shell integrity, fracture resistance, and desiccation tolerance were evaluated between populations from control and CO2 vent sites. We found no effects of reduced pH on population parameters or desiccation tolerance across the pH gradient, but significant differences in shell morphology, shell integrity, and fracture resistance were detected. Individuals from the CO2 vent site exhibited a higher shell aspect ratio, greater percentages of shell dissolution and break, and compromised shell strength than those from the control site. Our results highlight that long-term exposure to high pCO2 can negatively affect the shell features of P. sauciatus but may not have a significant effect on population performance. Moreover, we suggest that loss of shell properties could lead to changes in predator-prey interactions.

Comparative evaluation of the tissue dissolution capability of 3% of sodium hypochlorite, 5%pomegranate, and 5%miswak

Objective: This study aimed to evaluate of the tissue dissolution capability of 3% of sodium hypochlorite, 5%pomegranate, and 5% miswak.Methods: 45 freshly extracted premolar teeth were used. The teeth were grouped into three groups (n=15) Group I: The pulp tissue was immersed in 3% sodium hypochlorite irrigating solution. Group II: The pulp tissue were immersed in Punicagranatum (5%pomegranate) Nano particles irrigating solution. Group III: The pulp tissue were immersed in Salvadorapersica (5%miswak) Nano particles irrigating solution. The pulp tissue obtained was inserted into a small plastic test tube and 10ml of the irrigating solution were added to it and stored for 15 min. The ultrasonic tip were inserted inside the tube with irrigating solution and allowed to work for 1 minute to achieve proper agitation. After 15 min the solution was filtered through absorbing filter paper for 3 min to remove any excess moisture and left the sample to dry. Then the weight of the residual pulp tissue was measured and the difference between the initial and final weight was used to calculate the weight loss that were represent the dissolving power of each solution.Results: The highest value of dissolution percentage was found in Sodium hypochlorite group (98%), followed by Pomegranate group (78.3%). while the least value was found in Miswak group (66.8%). p= ≤0.001.Conclusion: On contrary of miswak, Pomegranate gives promising results in relation to NaOCl in terms of tissue dissolving capacity.

STATISTICAL INTERPRETATION AND OPTIMIZATION OF VALSARTAN FLOATING TABLETS USING BOX-BEHNKEN DESIGN

Objective: The main purpose of this study was to formulate and statistically evaluate 300 mg floating tablets of valsartan.
 Methods: Floating tablets of valsartan was prepared in 16 station rotary punching machine by considering 300 mg of valsartan as drug, 40-60 mg of hydroxypropyl methylcellulose (HPMC) K100M and 20-40 mg of poly (styrene-divinylbenzene) as polymers and 20 mg of sodium bicarbonate as gas generating agents. Since upper stomach has maximum therapeutic window for valsartan absorption, hence Gastroretentive Floating Tablets (GRFTs) was prepared by implementing Box-Bentham Design. The pre and post compression parameters were optimized using Statistica 10 software. From the in vitro buoyancy and drug release studies and interpretation of statistical outcomes viz. Akaike Information Criterion (AIC), Bayesian Information Criterion (BIC), Root Mean Squared Error (RMSE), Dissolution Efficiency (DE), Mean Dissolution Time (MDT), desirability study, it was concluded that batch VF5 formulation was found to be the most optimized formulation.
 Results: The floating time of VF5 was found to be 132±0.33 sec, in vitro buoyancy time was 18 h, Akaike Information Criterion (AIC) was 54.97, Bayesian Information Criterion (BIC) was 5.13, percentage dissolution efficacy was 56.39%, mean dissolution time was 5.19hr. Further, six-month stability study was performed as per ICH QIA guideline. After performing two-way ANOVA within stability study response variables, it was confirmed that the interaction was most significant.
 Conclusion: Valsartan floating drug delivery system was successfully developed by considering HPMC K100M and poly (styrene-divinylbenzene) as polymers. Among all the nine batches, VF5 was found to be the best-optimized batch.

Oxidative dissolution of nickel matte in dilute sulfuric acid solutions

Nickel matte (Ni3S2) is the most common feedstock for producing nickel oxide and nickel metal in associated refineries. Nickel matte is produced from sulfide or laterite ores, and contains around 73 wt% nickel. This study investigated the dissolution parameters of nickel matte in dilute sulfuric acid media in the presence of air as oxidant with the goal of presenting a cost-effective process for leaching nickel matte. The dissolution experiments were carried out to examine the following effects: air flow rate, stirring speed, S/L ratio, acid concentration, reaction temperature, reaction time and the amount of ferrous sulfate added. Nickel extraction of 90% and cobalt extraction of 80% were achieved using dilute H2SO4 and sparging of air as a source of oxygen. To increase the dissolution percentage of the matte, ferrous sulfate addition was studied and the oxidation and reduction potential (ORP) was measured to investigate the effect of ferrous ions on nickel and cobalt recovery. The highest nickel dissolution percentage (95%) was observed with the initial addition of 1200 mg/L Fe (II). Characterization of samples has been carried out with quantitative X-ray diffraction (XRD) and scanning electron microscopy, along with an energy dispersive system (SEM-EDS).

Development and evaluation of liquid crystal systems of combination of 5-fluorouracil and curcumin for cervical cancer cell line

Context: Liquid crystalline gel, self-assembled vesicular systems covered with nonionic surfactants, are promising for use in drug delivery. Aims: To develop and evaluate the liquid crystal (LC) systems of a combination of 5-fluorouracil and curcumin for a cervical cancer cell line. Methods: The LC was formulated using water, surfactant, and glycerin. Optimization was carried out by using different surfactants. The formulations were chosen for various studies, such as pH determination, environmental scanning electron microscopy (eSEM), Fourier transform infrared spectroscopy (FTIR) and dissolution study. The synergism of the combination of 5-FU and curcumin on cervical cancer HeLa cell line was then analyzed using CompuSyn software. Results: The formulations with 60% surfactant, the average particle size was in the ranges from 15.68 – 26.35 nm whereas with 40% surfactant, were 11.27 - 21.35 nm. The percentage of dissolution of 5-FU at pH 7 (PBS) A2: 40.23 > B2: 47.39 > X2: 50.36 > Y2: 56.36 compared to at pH 4 (vaginal simulated fluid, VSF) were A2: 36.23 > B2: 43.64 > X2: 45.67 > Y2: 49.01. The percentage of dissolution of curcumin of different formulations were at pH 7 (PBS) A2: 44.85 > B2: 51.36 > X2: 58.61 > Y2: 64.38 compared to at pH 4 (VSF) were A2: 41.03 > B2: 49.37 > X2: 57.85 > Y2: 68.75. Conclusions: The combination of the drugs showed that there was a synergistic effect when it was being administered together. The combination of drugs in LC system had a sustained release as well as it was effective against cervical cancer HeLa cell line.

Role of the location and size of soluble particles in the mechanical behavior of collapsible granular soil: a DEM simulation

Collapsing soil structure caused by mineral dissolution is a challenge to geoenvironmental projects. Although the parameters affecting the macro-response of collapsible soil have been addressed experimentally, the micromechanical behavior of soluble soil is unclear. The aim of this study was to simulate the dissolution behavior of a granular assembly at the particle level. A DEM code was developed that considers both localized and random dissolution as well as the particle size distribution and stress level. The effect of particle dissolution was simulated by considering the role of particle size in the load-bearing skeleton. The results show that mechanical behavior of a granular assembly is strongly influenced by the location and percentage of dissolution of particles. The loss of the soluble particles decreases physical contact and transfers to neighboring particles due to the arching forces around the voids, as in a honeycomb structure. However, if the soluble areas cut across the load-bearing force chains, a honeycomb fabric cannot form because of the lack of an arching effect, leading to the collapse of the structure and large volume change. Particle loss of up to 3% will not have a serious impact on the mechanical behavior of the granular assembly. After fine particle dissolution of a binary mixture, the arching effect around them decreases the volumetric strain in comparison with the dissolution of coarse particles. Also, during dissolution, the high stress level will decrease the peak friction angle, but the opposite is true for the post-dissolution behavior above 12% strain.

PREPARATION, CHARACTERIZATION, AND EVALUATION OF ANTI-INFLAMMATORY ACTIVITY OF ETORICOXIB LOADED SOLUPLUS® NANOCOMPOSITES

Objective: The objective of this study was to prepare and characterize etoricoxib (ECB) loaded Soluplus® nanocomposites to improve its physicochemical properties. The effect of polymer and surfactant concentration on particle size, in vitro percentage dissolution efficiency and the anti-inflammatory activity of nanocomposites were also investigated.Methods: The nanocomposites were prepared by using a freeze-drying technique. The analytical evidence for the formulation of lyophilized nanocomposites in solid state were generated and confirmed by differential scanning calorimetry (DSC), fourier transformation infrared spectroscopy (FTIR), x-ray powder diffractometry (XPRD) and scanning electron microscopy (SEM). The in vitro drug release profile of nanocomposites was compared with pure ECB powder.Results: The nanocomposites of ECB were contained in a nano range with particle size and zeta potential of 63.5 nm and 46.5 mv, respectively. The solubility and dissolution of the nanocomposites were significantly (p<0.001) improved as compared to ECB alone, evidenced by decreased log P values (1.90±0.002) of the nanocomposites. The characterization studies revealed the formation of amorphous nanocomposites of ECB with existence of physical interactions between drug and polymer. The anti-inflammatory activity of nanocomposites evaluated by carrageenan-induced rat paw edema model demonstrated nonsignificant (p>0.05) increase in anti-inflammatory activity as compared to pure ECB.Conclusion: From the results, it could be concluded that the formation of ECB nanocomposites with Soluplus® could be an effective and alternative approach to modify the physicochemical properties of ECB.

Paclitaxel-betulinic acid hybrid nanosuspensions for enhanced anti-breast cancer activity

Paclitaxel-betulinic acid hybrid nanosuspensions (PTX-BA-NP) with increased anti-breast cancer activity were developed. The resultant nanosuspensions (NP) had a mean particle size of 282.54 ± 5.4 nm, a polydispersity index of approximately 0.242 ± 0.02, a zeta potential of -19.7 ± 0.19 mV and a redispersibility index of 103.3 ± 0.01%. The cumulative dissolution percentage of PTX coarse powder and PTX-BA-NP dried powder at 60 min were 15.4% and 90.8%, respectively. MCF-7 cell-based testing showed that treatment with PTX-BA-NP led to more PTX-BA-NP accumulation in the cytoplasm of breast cancer cells, less cell cycle arrest in the G2-M phase, more cell cycle arrest in the G0-G1 phase, more apoptosis-induced cell death and stronger inhibition of cell migration than paclitaxel nanosuspensions (PTX-NP). Biodistribution studies showed that tumor accumulation levels at 12 h in the PTX-BA-NP group were approximately 2.67- and 2.33-fold higher than the levels in the Taxol® and PTX-NP groups, respectively. In vivo antitumor efficacy demonstrated that PTX-BA-NP exerted the strongest tumor inhibition among the four groups, with a tumor inhibition rate of 47.79 ± 2.28%, followed by PTX-NP (35.05 ± 5.55%), Taxol® (22.67 ± 6.01%) and betulinic acid nanosuspension (BANP) (14.38 ± 6.02%). These findings indicate that PTX-BA-NP holds great promise for breast cancer therapy.

Overcoming Poor Solubility of Dimenhydrinate: Development, Optimization and Evaluation of Fast Dissolving Oral Film.

Purpose: To develop fast dissolving oral film to address vomiting and nausea in pediatric population.Methods: Oral films of Dimenhydrinate were prepared by solvent casting method by using hydroxypropylmethyl cellulose E5 (HPMC E5), polyethylene glycol 400 (PEG 400) and croscarmellose sodium. Solubility of dimenhydrinate was enhanced by ethanol as a co-solvent. To make dimenhydrinate palatable sodium saccharin and peppermint oil were used. All films were evaluated for mechanical parameters, surface pH, morphology, disintegration time and percent dissolution.Results: Films were smooth, acceptable and white in colour. For optimized batch, drug content (99.106%), disintegration time (25 sec), dissolution (99.10% in 210 sec), surface pH (6.81) were acceptable.Conclusion: Optimized batch, due to its potential to deliver through fast dissolving film, can be developed for clinical use.