Complex Behavior of Bile Salts (SC and SDC) at Various Temperatures under the Influence of Tricyclic Antidepressant Drug (Imipramine) in Aqueous Solution

Surfactants play important role in almost every sector of industry like oil recover, pharmaceutical, physical and organic chemistry, cosmetic industry, food science etc. Micelles have importance property in various industries but basically it play important role in pharmaceutical industry because it have ability to dissolve sparingly soluble active substance like drug in aqueous solution. Introduction


Introduction
Important role of micelle is in delivery of drug towards targeted area and increase its bioavailability. It also attempt to minimize drug degradation, its loss, and to prevent its harmful side effects [1].
Micelles as drug carriers present some advantages when compared to other alternatives such as soluble polymers and liposomes. Micellar systems can solubilize poorly soluble drugs and thus increase their bioavailability, they can stay in the body (blood) long enough to provide gradual accumulation in the required area, and their sizes permit them to accumulate in areas with leaky vasculature [2].
In general, surfactants play an important role basically in pharmaceutical biotechnology fields, since they are largely utilized in various drug dosage forms to control wetting, stability, bioavailability, among other properties [3]. It is important to notice that lyophobic colloids, such as polymers, require certain energy to be applied for their formation, are quite unstable from the thermodynamic point of view, and frequently form large aggregates. Association colloids such as micelles, on the other hand, can form spontaneously under certain conditions (selfassembling systems), and are thermodynamically more stable towards both dissociation and aggregation [4].
In this work, we provide a review of micellar solubilisation of drugs in surfactant systems, blending it with basic information on surfactants structure and properties, as well as the applications for drug delivery. The main aim of our investigation was to study the influence of varying structures of the hydrophobic regions of selected anionic surfactants on the physico-chemical properties and the synergism effect in the bile salt and -anionic binary systems (Figures 1-3).

Experimental Material
The bile surfactant Sodium Cholate (SC) and Sodium Deoxycholate (SDC) having anionic nature which is used in experiment was produced from LOBA Chemic and Imipramine. All the solutions were prepared in triple distilled water.

Determination of critical micellization concentration value of binary mixtures
In this experiment micellization tendency is determined by conductometric method because pure water or unionized water is a good insulator of electricity. If any charge or soluble ions present in it then it allow to flow current through aqueous solution thus the amount of current flow is used to calculate its ionic concentration (Tables 1 and 2).
The Critical Micelle Concentration (CMC) of the binary mixtures (Bile salt and Drugs) were studied using conductivity measurements, at different mole fractions and different temperature [5] prepared mixtures consisted of 0.1-1 mole fractions of SC and SDC and 0.1 mole fraction of Imipramine (Figures 4-9).
The CMC values for individual non-ionic surfactants and Imipramine were obtained through conductometric measurements ( Table 3).

Thermodynamics of micellization
Surfactant concentration is increases gradually after some time it reaches at particular concentration which shows deviation between pre micellar region and post micellar region known as CMC, from where micelle form is spontaneous. This means the free energy of surfactants molecule of micelle is always be less than the monomeric surfactants molecule when dissolving in distilled water. All the thermodynamics parameters are temperature dependent [6].
The Gibbs free energy of micellization ΔGᵒ m was calculated by using following equation- The Calculated value of parameter is shown in Tables 4 and 5 Sodium Cholate (SC).      at various temperature range. The ∆Gᵒ m is decrease with increasing temperature, this value show that the micellization process is spontaneous in aqueous mixtures and magnitude of hydrophobic effect is increases with increasing temperature (Tables 4 and 5) [6].
The ∆Hᵒ m can be derived by the Von't Hoff equation.
The result also shows that standard enthalpy of micellization is negative which indicates that the micelle formation process is exothermic which show strong interaction between drug and bile salts [6].

Concentration SC (mM)
To determination of CMC of Sodium Cholate (0.08 N) and Imipramine (0.1 N) in aqueous solution at room temperature. Determination of CMC of Sodium Cholate (0.06 N) and Imipramine (0.1 N) in aqueous solution at 310 K temperature.

Specific conductivity [mS] concentration of SDC [mM]
Determination of CMC of Sodium Cholate (0.02 N) and Imipramine (0.1 N) in aqueous solution at 310 K temperature.

Figure 6
Determination of CMC of Sodium Deoxycholate (0.08 N) and Imipramine (0.1 N) in aqueous solution at 320 K temperature.

Figure 7
International Journal of Applied Science -Research and Review ISSN 2349-7238 cmc id , x id , X 1 and the β parameter all were calculated by using following equation [1,7]. The cmc id parameter indicates non-ideal behaviour if it differs from cmc ex . The values of x id and the x 1 are used to calculate the β parameter. Critical micelle concentrations according to Clint's theory of ideal mixtures (cmc id ) in Tables 6  and 7.
The cmc id values are presented and compared to the experimental CMC (cmc ex ) in Tables 8 and 9 [7]. Deviation of the experimentally obtained CMC values from those calculated according to Clint's theory indicates non-ideal behaviour of examined surfactant mixtures and mutual interactions of the surfactants in the micelles. according to this experimental CMC are always be smaller than those predicted using models. The mole fraction of the more hydrophobic surfactant in the ideal mixed micelle (x id ), according to Motomura [10,11] was calculated using the following relationship: The x 1 value was calculate by using following relation: The x id and the x 1 values for the mixed micelles are presented in Tables 8 and 9. Further according to Rubingh equation [7,12] 1x 1 value was used to calculate the β interaction parameter, through the following equation: (1-x) α β β values explain the synergism or antagonism between two surfactants in mixed micelles. Its negative value indicate attractive interactions (synergism) between components of mixed micelles of drug and bile salt, The less negative value means the weaker synergistic interaction while positive values shows antagonistic interactions between surfactants in a mixture. Its value also shows the deviation between experimentally obtained (cmc ex ) and calculated (cmc id ) cmc values [7].

Conclusion
Binary combinations of bile salt and antidepressant drug (Imipramine) as well as their tendency to form mixed micelles having CMC's different than ideal conditions, the non ideality is more for the binary mixtures. The binary mixture of both surfactants and drug mixture was analysed by conductometer methods. The results of the study have been analysed using Clint's, Rubingh's, and Motomura's theories for mixed binary systems [13]. The Critical Micelle Concentration (CMC) of the ideal mixed micelle, the mole fraction of the more hydrophobic surfactant in the ideal mixed micelle, the mole fraction of the more hydrophobic surfactant in the real mixed micelle, and the -TΔSᵒ m = (ΔGᵒ m -ΔHᵒ m ) The ΔSᵒ m is always being positive which indicate that the process of micellization is entropy dominated over the micelle formation process. The positive value of ΔSᵒ m is due to the hydrophobic interaction between the surfactants and water molecule [ 6,7].

Development of model
The present study provides an insight into the mechanism of interaction of bile salts with various drugs like Imipramine. Based on the experimental findings it is possible to propose the concentration ranges involved with different stages of changes in the solubilisation of drugs by SC and SDC. The experiments showed that the concentration of a bile salt needed to bring about a certain change in the drugs is strongly dependent on the absolute concentrations of bile salt and not on their molar ratio. The bioavailability of orally administered drugs can be influenced by interacting with food constituent and by physico-chemical conditions in the upper gastrointestinal tract. Normally, bile salts enhance the transport of lipophilic drugs across mucosal membranes. Bile salts are able to form stable mixed micelles consisting of fatty acids and phospholipids. Conventional micellar systems are known to solubilize lipophilic drugs having a low bioavailability [8].
Surfactant (bile salt) added in the drug and distilled water solution, and then the dissolution rate of the Imipramine tablets increases (Tables 1 and 2). It concludes that even presence of small concentration of bile salts is very helpful for the dissolution of various drugs [9].
In method to observing the influence of the structure of drug on formation of mixed micelles [5] with SDC and SC, physicochemical values of micelles and mixed micelle were calculated by using experimental CMC values which is shown in Tables 4 and 5. Respective plot of specific conductivity and concentration of 0.08 mM Imipramine at various temperatures.      β interaction parameter of the mixed micelles were calculated by using experimental values obtained [5]. It was concluded that increased synergistic interactions can be due to the larger number of hydrophilic groups present in the drug and bile salt.   Table 9 Value of cmc id /mM, cmc ex /mM, X id and X 1 and the β of the mixed micelles of Imipramine and anionic surfactants (SC) at different mole fractions in aqueous solution.