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Pharmaceutical Chemistry 500 Topics For Project Report
Pharmaceutical Chemistry Project Topics List (1–100)
1. Synthesis and characterization of novel anti-inflammatory agents
2. Design and synthesis of benzothiazole derivatives for anticancer activity
3. Development of a validated HPLC method for simultaneous drug estimation
4. Molecular docking studies of antiviral drug candidates
5. Green synthesis of metal nanoparticles and their pharmaceutical applications
6. Spectrophotometric estimation of combination drugs in dosage forms
7. QSAR analysis of antimalarial drug analogues
8. Isolation and characterization of bioactive compounds from medicinal plants
9. Formulation and evaluation of sustained-release dosage forms
10. Synthesis of Schiff base complexes and biological evaluation
11. Development of forced degradation methods for stability studies
12. Design and synthesis of heterocyclic analogues for antibacterial activity
13. Evaluation of antioxidant potential of newly synthesized compounds
14. Synthesis of coumarin derivatives as potential anticancer agents
15. Analytical method validation according to ICH guidelines
16. Comparative study on solubility enhancement techniques
17. Synthesis of indole derivatives as antimicrobial agents
18. Spectroscopic determination of impurities in bulk drugs
19. Formulation and characterization of nanoparticles for targeted delivery
20. Study of degradation kinetics of selected antibiotics
21. Microwave-assisted synthesis of heterocyclic compounds
22. Analytical profiling of fixed-dose combination drugs
23. Computational modeling of enzyme inhibitors
24. Synthesis and biological screening of pyrazole derivatives
25. Determination of drug–excipient compatibility using FTIR
26. Analytical quantification of impurities using LC-MS
27. Synthesis of oxadiazole derivatives for antifungal activity
28. Comparative dissolution studies of marketed formulations
29. Study of photostability and degradation products of drugs
30. Design and synthesis of thiazole-based molecules for anti-TB activity
31. RP-HPLC method development for multicomponent formulations
32. Bioavailability enhancement through solid dispersion technique
33. Synthesis of pyridine derivatives with analgesic activity
34. Validation of analytical methods for impurity profiling
35. Synthesis of benzimidazole analogues for anti-ulcer activity
36. Stability-indicating method development for antihypertensive drugs
37. Synthesis and pharmacological screening of oxazole derivatives
38. Chemical modification of natural compounds for improved efficacy
39. Forced degradation studies on antiretroviral drugs
40. Development of spectrofluorimetric methods for trace analysis
41. Synthesis of substituted quinoline derivatives for antimicrobial activity
42. Characterization of polymorphic forms in active pharmaceutical ingredients
43. Spectrophotometric analysis of binary drug mixtures
44. Synthesis of pyrazoline derivatives with antidiabetic potential
45. Study of pH-dependent drug degradation
46. Synthesis and docking of new anti-Alzheimer compounds
47. Quantitative estimation of preservatives in formulations
48. Green analytical method for estimation of pharmaceutical residues
49. Design and synthesis of hybrid heterocyclic scaffolds
50. Analysis of degradation impurities using LC-MS/MS
51. Synthesis of triazole analogs for antifungal activity
52. Validation of RP-HPLC methods for multicomponent drugs
53. Analytical study of degradation products in stress testing
54. Development of stability-indicating UV methods
55. Synthesis of quinazoline analogues for antitubercular activity
56. Determination of heavy metals in herbal drug formulations
57. Molecular docking analysis of COX-2 inhibitors
58. Synthesis of oxindole derivatives for anticonvulsant activity
59. Analytical comparison between branded and generic formulations
60. Formulation and characterization of inclusion complexes
61. Study on forced degradation of vitamins in supplements
62. Synthesis of coumarin–thiazole hybrids
63. Quantification of residual solvents using gas chromatography
64. Analytical method development for herbal constituents
65. Synthesis and evaluation of benzofuran derivatives
66. Spectrophotometric estimation of multicomponent dosage forms
67. Determination of partition coefficients of novel drug molecules
68. Forced degradation and impurity profiling in tablets
69. Synthesis of hydrazide–hydrazone derivatives as antimicrobial agents
70. Analytical estimation of preservatives in ophthalmic products
71. Design and synthesis of sulfonamide analogues
72. RP-HPLC method development for simultaneous estimation in plasma
73. Synthesis of indazole derivatives for anti-inflammatory activity
74. Validation of cleaning procedures in pharmaceutical production
75. Synthesis of benzoxazole derivatives for anti-HIV activity
76. Study on solid-state degradation of drugs
77. Analytical quantification of antioxidants in formulations
78. Synthesis and evaluation of Schiff base metal complexes
79. Chemical stability of vitamins in nutritional products
80. Formulation and evaluation of fast-dissolving tablets
81. Synthesis of oxazole–pyrimidine hybrids for antimicrobial screening
82. Analytical determination of impurities formed during drug degradation
83. Synthesis of 1,3,4-thiadiazole analogues for antibacterial action
84. Development of QbD-based analytical method for validation
85. Forced degradation and mass spectral identification of impurities
86. Synthesis of heteroaryl hydrazones for anti-inflammatory activity
87. Quantitative analysis of excipients in dosage forms
88. Synthesis of chalcone derivatives and antioxidant screening
89. Spectrophotometric estimation of drug content in plasma
90. Green synthesis of heterocycles via solvent-free reactions
91. Synthesis of substituted pyrimidines for anticancer evaluation
92. Analytical profiling of nutraceutical products
93. Synthesis of new oxadiazole–pyrazole hybrids
94. Forced degradation studies under acidic and alkaline conditions
95. Synthesis of triazine analogues for antimicrobial activity
96. Stability studies of emulsified formulations
97. Analytical estimation of vitamin content using HPLC
98. Synthesis of pyrazoloquinoline derivatives for CNS activity
99. Spectroscopic analysis of drug–metal complexation
100. Quantitative estimation of trace impurities using ICP-MS
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Pharmaceutical Chemistry Project Topics List (101-200)
101. Synthesis of benzimidazole–pyridine hybrids
102. LC-MS determination of degradation products
103. Analytical evaluation of herbal versus synthetic combinations
104. Synthesis of new anti-oxidant Schiff bases
105. Study of forced degradation under photolytic conditions
106. Analytical profiling of drug impurities as per ICH Q3A
107. Synthesis of heterocyclic analogs for anti-HIV screening
108. Quantification of excipient-related degradation products
109. Synthesis and evaluation of benzothiazole–oxadiazole hybrids
110. Molecular modeling and docking of kinase inhibitors
111. Synthesis of thiazolidinone derivatives for antidiabetic activity
112. RP-HPLC method development for impurity profiling
113. Determination of active ingredients in transdermal patches
114. Synthesis of indole-based thiosemicarbazone analogues
115. Forced degradation studies using QbD approach
116. Synthesis of hybrid heterocycles via multicomponent reactions
117. Spectrophotometric analysis of binary mixtures
118. Development of stability-indicating LC methods
119. Synthesis of coumarin–quinoline analogues
120. Analytical estimation of metal impurities in APIs
121. Validation of methods for biological samples
122. Synthesis of pyridine–benzimidazole hybrids for antimicrobial testing
123. Forced degradation and impurity mapping by LC-MS
124. Synthesis and biological evaluation of pyrazole–thiazole hybrids
125. Analytical estimation of preservatives in cosmetic formulations
126. Formulation and analysis of solid lipid nanoparticles
127. Synthesis of quinoline–triazole derivatives
128. Spectrophotometric evaluation of marketed formulations
129. Synthesis of benzofuran–oxadiazole analogs
130. Analytical determination of chiral drugs using HPLC
131. Forced degradation and mass balance studies
132. Synthesis of thiophene–pyrimidine hybrids
133. Development of UV spectroscopic method for drug quantification
134. Synthesis of pyrimidinone derivatives for antiviral evaluation
135. Quantitative estimation of impurities in parenteral dosage forms
136. Analytical study of drug degradation under humidity stress
137. Synthesis of oxadiazole–benzothiazole analogs
138. Study on degradation kinetics of multivitamin combinations
139. Synthesis of triazole–quinazoline derivatives
140. LC-MS analysis of forced degradation products
141. Synthesis of oxindole–pyrrole hybrids for anticancer potential
142. Spectrophotometric estimation of multiple active ingredients
143. Synthesis of new heterocycles using ionic liquids
144. Validation of analytical methods for biological matrices
145. Synthesis of benzothiazole–pyrazole hybrids
146. Study on photostability and oxidation degradation of drugs
147. Synthesis and antimicrobial evaluation of thiazole analogues
148. Forced degradation and impurity identification in antibiotics
149. Analytical determination of preservatives in syrups
150. Synthesis of oxazole–pyridine hybrids
151. Development of validated HPLC methods for antiviral drugs
152. Quantification of degradation impurities by LC-MS/MS
153. Synthesis of benzofuran–thiazole analogues for antioxidant activity
154. Forced degradation of antihypertensive combination drugs
155. Analytical estimation of excipient degradation by-products
156. Synthesis and evaluation of quinoline–indole hybrids
157. Characterization of crystalline polymorphs using XRD
158. Synthesis of pyrimidine–oxadiazole derivatives
159. Analytical profiling of antidiabetic drug formulations
160. Synthesis of indazole–triazole hybrids
161. Forced degradation and structure elucidation by NMR
162. Analytical estimation of vitamin degradation kinetics
163. Synthesis of oxadiazole–thiazole analogues
164. Validation of UV methods for fixed-dose combinations
165. Synthesis and antioxidant screening of chalcone–pyrrole hybrids
166. Spectrophotometric estimation of paracetamol and caffeine
167. Synthesis of benzimidazole–pyrazole hybrids for antimicrobial use
168. Stability studies of ophthalmic formulations under stress
169. Synthesis of quinoline–triazine hybrids for anti-TB testing
170. Analytical profiling of degradation products in injectables
171. Synthesis of oxazole–thiadiazole derivatives
172. Development of impurity profiling methods by HPTLC
173. Synthesis of indole–coumarin analogues for anticancer use
174. Forced degradation study of lipid-based formulations
175. Analytical determination of metal contaminants
176. Synthesis of pyridine–thiazole hybrids for anti-inflammatory screening
177. LC-MS study of stress degradation impurities
178. Synthesis of oxadiazole–pyridine analogues
179. Quantitative estimation of excipients by spectrophotometry
180. Synthesis of benzofuran–triazine hybrids for antimicrobial testing
181. Analytical study on antioxidant stability in multivitamins
182. Synthesis of triazole–coumarin analogues for antifungal use
183. Forced degradation of antibiotics under oxidative conditions
184. Analytical profiling of herbal–synthetic drug combinations
185. Synthesis of oxazole–indole hybrids
186. Validation of analytical method for complex dosage forms
187. Synthesis of thiazole–pyrimidine derivatives for anticancer testing
188. LC-MS identification of degradation products
189. Synthesis of benzothiazole–quinoline hybrids
190. Spectrophotometric estimation of ternary mixtures
191. Synthesis and biological evaluation of oxadiazole analogues
192. Forced degradation studies on lipid nanoparticles
193. Synthesis of indole–triazine analogues
194. Development of green chromatographic methods
195. Synthesis of coumarin–benzimidazole hybrids
196. Analytical estimation of excipient interaction products
197. Synthesis of oxazole–quinazoline derivatives
198. Validation of HPLC methods for multicomponent analysis
199. Synthesis of pyrimidine–triazole hybrids for antiviral studies
200. Stability studies of antimalarial formulations
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Pharmaceutical Chemistry Project Topics List (201-300)
201. Synthesis of indazole–benzothiazole analogues
202. Forced degradation profiling of herbal drug mixtures
203. Synthesis of thiazole–oxindole hybrids
204. Spectrophotometric estimation of painkiller combinations
205. Synthesis of oxadiazole–quinoline derivatives
206. Analytical estimation of impurities by UV-visible methods
207. Synthesis of benzothiazole–pyrimidine hybrids
208. Forced degradation studies under thermal conditions
209. Synthesis of triazole–indole hybrids
210. Analytical evaluation of nutraceutical degradation kinetics
211. Synthesis of coumarin–pyrimidine derivatives
212. Spectroscopic analysis of metal–drug coordination complexes
213. Synthesis of oxazole–benzofuran hybrids
214. Validation of green spectrophotometric methods
215. Synthesis of indole–quinazoline derivatives
216. Forced degradation of cardiovascular drug formulations
217. Synthesis of thiazole–quinoline hybrids
218. Analytical profiling of degradation in topical formulations
219. Synthesis of oxadiazole–benzothiazole hybrids
220. Spectrophotometric estimation of antihistamine mixtures
221. Synthesis of benzofuran–quinazoline analogues
222. Forced degradation under oxidative stress conditions
223. Synthesis of pyrimidine–indole analogues
224. LC-MS identification of forced degradation impurities
225. Synthesis of oxazole–benzothiazole hybrids
226. Validation of analytical methods for biologics
227. Synthesis of indazole–quinoline analogues
228. Analytical determination of antioxidants in cosmetic preparations
229. Synthesis of thiazole–benzofuran hybrids
230. Forced degradation of multivitamin formulations
231. Synthesis of coumarin–indole hybrids
232. Spectrophotometric estimation of antipyretic combinations
233. Synthesis of oxadiazole–quinazoline analogues
234. LC-MS profiling of stress degradation products
235. Synthesis of benzothiazole–oxazole hybrids
236. Analytical evaluation of antioxidants in oil-based systems
237. Synthesis of triazine–quinoline hybrids
238. Forced degradation and impurity quantification
239. Synthesis of indole–benzofuran analogues
240. Analytical estimation of preservatives in cosmetic creams
241. Synthesis of thiazole–pyridine hybrids
242. Validation of spectrophotometric assay for combination drugs
243. Synthesis of oxadiazole–indole hybrids
244. Forced degradation study of protein-based formulations
245. Synthesis of coumarin–quinazoline hybrids
246. Spectrophotometric determination of anti-inflammatory combinations
247. Synthesis of benzofuran–thiazole analogues
248. Analytical profiling of degradation in emulsions
249. Synthesis of oxazole–indole analogues
250. LC-MS determination of trace degradation impurities
251. Design and Synthesis of Thiazole Derivatives as Potent Antifungal Agents
252. Analytical Validation of RP-HPLC Method for Determination of Antihypertensive Drugs
253. Study on Kinetics and Mechanism of Drug Degradation under Stress Conditions
254. Development of Novel Pyridine-Based Antibacterial Compounds
255. Synthesis and Characterization of Schiff Base Metal Complexes with Biological Activity
256. Comparative Evaluation of Solvent Extraction Techniques for Alkaloid Isolation
257. Investigation of Bioavailability Enhancement using Solid Dispersion Techniques
258. Synthesis of Coumarin Derivatives as Anti-inflammatory Agents
259. Spectroscopic Analysis of Drug–Protein Interactions
260. Study on Drug Polymorphism and Its Impact on Bioavailability
261. Preparation and Characterization of Polymeric Prodrugs
262. Synthesis of 1,3,4-Oxadiazole Derivatives as Anticonvulsant Agents
263. Development of pH-Sensitive Drug Delivery Polymers
264. Analytical Method Development for Determination of Impurities in Antibiotics
265. Synthesis and Pharmacological Evaluation of Quinazoline Derivatives
266. Design and Characterization of Novel Anticancer Lead Compounds
267. Study of Forced Degradation Behavior of Pharmaceutical Formulations
268. Evaluation of In Vitro Cytotoxicity of Synthesized Compounds
269. Synthesis and Biological Evaluation of Thiadiazole Analogues
270. Analytical Profiling of Multi-Component Drug Formulations
271. Study on Drug Release Kinetics from Hydrophilic Matrices
272. Investigation of the Role of Metal Ions in Drug Binding
273. Development of Stability-Indicating Analytical Methods
274. Molecular Docking Analysis of Newly Designed Drug Candidates
275. Formulation and Characterization of Nanocrystals for Poorly Soluble Drugs
276. Synthesis and In Vitro Screening of Pyrazole Derivatives
277. Determination of Drug Residues in Environmental Samples
278. Study on the Influence of Temperature on Drug Stability
279. Synthesis of Benzothiazole Derivatives as Anti-Tubercular Agents
280. Analysis of Dissolution Kinetics in Modified Release Tablets
281. Quantitative Analysis of Active Pharmaceutical Ingredients in Tablets
282. Synthesis of Sulfonamide Derivatives with Antiviral Activity
283. Study on Molecular Properties Influencing Drug–Receptor Binding
284. Development of UV-Visible Spectrophotometric Methods for Drug Estimation
285. Analytical Determination of Preservatives in Pharmaceutical Formulations
286. Formulation and Evaluation of Novel Drug Delivery Nanocarriers
287. Synthesis of Piperazine-Based Analogs for Neuroprotective Activity
288. Development of RP-HPLC Methods for Multi-Component Drugs
289. Synthesis and Screening of New Hydrazone Derivatives
290. Study on the Stability of Vitamins in Combined Formulations
291. Formulation Optimization using Design of Experiments (DoE)
292. Analytical Estimation of Pesticide Residues in Medicinal Plants
293. Synthesis of Triazole Derivatives with Antifungal Properties
294. Investigation on pKa Determination and Its Impact on Drug Solubility
295. Study on Drug–Surfactant Interactions for Enhanced Solubility
296. Design and Evaluation of Biodegradable Polymers for Drug Delivery
297. Synthesis of Quinoline Derivatives for Antiplasmodial Activity
298. Development of Analytical Methods for Drug Metabolites
299. Study on Solvent Polarity Effects on UV Absorption Spectra
300. Synthesis and Evaluation of Antioxidant Heterocyclic Compounds
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Pharmaceutical Chemistry Project Topics List (301-400)
301. Determination of Partition Coefficient of Newly Synthesized Drugs
302. Analytical Profiling of Drug Formulations by LC-MS
303. Synthesis of Novel NSAID Derivatives to Reduce GI Side Effects
304. Characterization of Impurity Profiles in API Production
305. Synthesis and Screening of Isoxazole Derivatives as Analgesic Agents
306. Determination of Heavy Metals in Pharmaceutical Products
307. Formulation of Soluble Drug Complexes using Cyclodextrins
308. Study of Antioxidant Activity of Synthetic Phenolic Compounds
309. Synthesis and Biological Screening of Pyrazoline Analogues
310. Quantitative Determination of Drugs in Biological Fluids
311. Analytical Method Validation for Stability-Indicating Parameters
312. Synthesis of Pyrimidine Derivatives as Antitubercular Agents
313. Study on Kinetic Parameters in Drug Stability Testing
314. Development of Analytical Procedures for Drug Combination Products
315. Synthesis of Indazole Derivatives as CNS Depressants
316. Investigation of Drug Partitioning in Biorelevant Media
317. Formulation and Evaluation of Lipid-Based Drug Carriers
318. Analytical Profiling of Polymorphic Drug Substances
319. Synthesis of Benzimidazole Derivatives for Anticancer Potential
320. Study on the Effect of pH on Drug Ionization and Absorption
321. Development of a New Analytical Method for Drug Impurity Quantification
322. Synthesis and Characterization of Pyrazolone Derivatives
323. Analytical Determination of Active Constituents in Herbal Medicines
324. Study of Drug Compatibility in Combination Therapies
325. Synthesis of New Fluoroquinolone Derivatives
326. Analytical Evaluation of Dissolution Profile of Sustained-Release Tablets
327. Development of Forced Degradation Studies for Analytical Method Validation
328. Synthesis and Biological Screening of Coumarin Derivatives
329. Spectrophotometric Analysis of Multicomponent Formulations
330. Investigation on Solubility Enhancement via Co-crystallization
331. Analytical Estimation of Drug Residues in Milk and Food Products
332. Synthesis of Benzofuran Derivatives for Anti-inflammatory Activity
333. Study of Polymorphism in Solid-State Drugs
334. Analytical Characterization of Drug–Excipient Interactions
335. Synthesis of Novel Hybrid Molecules with Dual Activity
336. Evaluation of Antimicrobial Potency of Synthesized Compounds
337. Analytical Quantification of Trace Impurities in Formulations
338. Study on Crystallinity and Its Effect on Drug Solubility
339. Synthesis of Isoquinoline Derivatives as Antimalarial Agents
340. Formulation of Microemulsions for Enhanced Drug Absorption
341. Analytical Determination of Drug Release from Polymeric Films
342. Synthesis of Benzoxazole Derivatives as Anti-HIV Agents
343. Study on Degradation Pathways of Cephalosporin Antibiotics
344. Development of Stability Protocols for Biological Drug Substances
345. Synthesis of Thiadiazine Derivatives with Antifungal Properties
346. Analytical Profiling of Drug Stability under Accelerated Conditions
347. Study of Partitioning Behavior in Lipid–Water Systems
348. Synthesis of Heteroaryl Compounds for Anti-inflammatory Activity
349. Analytical Estimation of Oxidative Degradation Products
350. Synthesis and Evaluation of New Analgesic Compounds
351. Characterization of API Using DSC and FTIR Techniques
352. Study on Dissolution Enhancement using Solid Lipid Nanoparticles
353. Synthesis of Pyrrole Derivatives as Antimicrobial Agents
354. Validation of HPTLC Method for Quantification of Herbal Drugs
355. Synthesis and Characterization of Imidazopyridine Derivatives
356. Analytical Profiling of Multidrug Formulations by HPLC
357. Synthesis of Thiazolidinone Derivatives for Antidiabetic Activity
358. Study on Degradation Kinetics of Drug–Excipient Systems
359. Synthesis of Novel Indole Derivatives for Neuroprotective Activity
360. Analytical Method Development for Dissolution Profile Testing
361. Evaluation of Antimicrobial Resistance Mechanisms in Drug Design
362. Synthesis and Evaluation of Benzothiazole Analogs
363. Study on Molecular Docking and Pharmacophore Mapping
364. Analytical Validation of Impurity Profiling Techniques
365. Synthesis of Triazine Derivatives with Anticancer Activity
366. Development of LC-MS Method for Drug Quantification
367. Synthesis and Characterization of Pyrimidinone Derivatives
368. Study of the Effect of Temperature and Humidity on Drug Degradation
369. Analytical Quantification of Drug Residues in Biological Matrices
370. Synthesis of Piperidine Derivatives for Antimalarial Activity
371. Validation of Analytical Methods for Chiral Separation
372. Synthesis of Oxindole Derivatives as Anticonvulsant Agents
373. Study on Drug Permeation through Biological Membranes
374. Analytical Estimation of Drugs Using Fluorometric Techniques
375. Synthesis of Isoxazoline Derivatives for Antibacterial Activity
376. Characterization of Drug Metabolites by LC-MS/MS
377. Synthesis and Biological Screening of Benzimidazole–Thiazole Hybrids
378. Study on the Effect of Surfactants in Drug Formulation
379. Analytical Determination of Solvent Residues in APIs
380. Synthesis of Benzoxazine Derivatives for Antiviral Potential
381. Formulation and Evaluation of Sustained Release Drug Systems
382. Analytical Estimation of Trace Metals in Formulations
383. Synthesis and Evaluation of 2-Amino Thiazole Derivatives
384. Study on the Role of Prodrugs in Targeted Drug Delivery
385. Synthesis of Pyridine Derivatives for Anti-inflammatory Activity
386. Analytical Profiling of Drug–Metabolite Ratios in Plasma
387. Synthesis and Characterization of Quinoline–Thiazole Hybrids
388. Study on Mechanism of Photodegradation in Drug Substances
389. Analytical Validation of LC Methods for API Quantification
390. Synthesis of Spiro Compounds for Antimicrobial Activity
391. Study on pH-Dependent Stability of Drug Molecules
392. Synthesis of Isoindoline Derivatives for Antipsychotic Activity
393. Development of Analytical Techniques for Controlled Release Drugs
394. Synthesis and Biological Screening of Triazole–Benzimidazole Hybrids
395. Characterization of Active Metabolites via Mass Spectrometry
396. Synthesis of Pyrazoline–Thiazole Derivatives as Anticancer Agents
397. Analytical Determination of Drugs in Urine and Plasma Samples
398. Study on Correlation Between Lipophilicity and Drug Activity
399. Synthesis of Benzothiazine Derivatives with Anti-inflammatory Potential
400. Analytical Method Development for Combination Drug Formulations
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Pharmaceutical Chemistry Project Topics List (401-500)
401. Synthesis and Characterization of Isoxazole–Thiazole Analogs
402. Investigation on the Influence of Salt Formation on Solubility
403. Analytical Estimation of Drugs Using Capillary Electrophoresis
404. Synthesis of Quinazoline–Piperazine Hybrids for Antibacterial Activity
405. Development of Stability-Indicating HPLC Methods for Peptides
406. Synthesis of Benzimidazole–Pyrazole Derivatives
407. Analytical Profiling of Drug Impurities Using UHPLC
408. Study on the Relationship Between Molecular Weight and Bioavailability
409. Synthesis of Thiazoloquinoline Derivatives for Antimalarial Activity
410. Validation of UV-Spectrophotometric Methods for Multi-Drug Analysis
411. Synthesis of Indole–Thiazole Derivatives for Antiviral Potential
412. Study on Mechanistic Aspects of Drug Metabolism
413. Analytical Estimation of Lipophilic Drugs in Biological Systems
414. Synthesis and Screening of Fused Heterocyclic Compounds
415. Analytical Determination of Degradation Products in Formulations
416. Synthesis of Oxazole–Thiazole Derivatives as Antifungal Agents
417. Development of Chromatographic Fingerprints for Herbal Drugs
418. Synthesis of Benzofuran–Thiazole Hybrids with Biological Potential
419. Study on Molecular Modeling for Enzyme Inhibition
420. Analytical Validation for Determination of Trace Impurities
421. Synthesis of Isoxazoline–Pyridine Derivatives as CNS Agents
422. Analytical Estimation of Antioxidant Drugs by HPLC
423. Synthesis and Evaluation of Benzoxazole–Pyrimidine Hybrids
424. Study on Drug Partition Coefficients in Simulated Biological Media
425. Analytical Determination of Stability of Peptide Drugs
426. Synthesis of Quinoline–Triazole Derivatives for Anticancer Activity
427. Formulation and Evaluation of Solubilized Drug Complexes
428. Analytical Profiling of Solid-State Drug Transformations
429. Synthesis of Pyrazole–Benzimidazole Derivatives
430. Study on the Impact of Ionic Strength on Drug Stability
431. Analytical Method Development for Drug Release from Liposomes
432. Synthesis of Pyrimidine–Thiazole Derivatives for Antitubercular Activity
433. Analytical Characterization of Crystalline vs. Amorphous Drugs
434. Synthesis and Evaluation of Quinazoline–Thiazolidinone Hybrids
435. Study on Drug–Carrier Interaction in Nanoparticle Formulations
436. Analytical Quantification of Bioactive Compounds in Plant Extracts
437. Synthesis of Fused Triazole–Benzofuran Compounds
438. Study on Photostability Testing of Drug Formulations
439. Analytical Determination of Drugs Using Derivative Spectroscopy
440. Synthesis and Characterization of New Schiff Base Analogs
441. Investigation of Ion Pair Formation in Drug Solubilization
442. Analytical Estimation of Drugs Using Potentiometric Titrations
443. Synthesis of Oxadiazole–Thiazole Derivatives
444. Study on pH–Solubility Profile of Weakly Basic Drugs
445. Analytical Profiling of Impurities Generated During Storage
446. Synthesis of Triazole–Coumarin Hybrids for Antimicrobial Potential
447. Validation of TLC Methods for Drug Purity Assessment
448. Synthesis and Characterization of Quinoline–Benzothiazole Hybrids
449. Analytical Study on Forced Degradation of Antimalarial Drugs
450. Synthesis of Isoxazole–Pyrimidine Derivatives for Antibacterial Activity
451. Analytical Quantification of Volatile Impurities in APIs
452. Study on Structure–Permeability Relationships in Drug Molecules
453. Synthesis of Pyrrole–Triazole Derivatives for Anti-HIV Activity
454. Analytical Method Development Using Green Chemistry Principles
455. Synthesis of Benzothiazole–Quinoline Derivatives for Anticancer Testing
456. Characterization of Solvent–Drug Interactions Using NMR
457. Analytical Profiling of Stability-Indicating Assays for Biologics
458. Synthesis of Thiazole–Indole Hybrids for Anti-inflammatory Potential
459. Study on Hydrogen Bonding Influence on Drug Solubility
460. Analytical Estimation of Trace Elements in Pharmaceuticals
461. Synthesis of Isoxazole–Quinazoline Derivatives
462. Development of Analytical Methods for Protein–Drug Conjugates
463. Synthesis and Characterization of Benzimidazole–Thiadiazole Hybrids
464. Study on the Mechanism of Metal–Drug Chelation
465. Analytical Profiling of Drug Formulations Under Freeze–Thaw Conditions
466. Synthesis of Pyrimidine–Benzothiazole Derivatives
467. Development of Methods for Determination of Enantiomeric Purity
468. Synthesis and Screening of New Thiazole–Benzofuran Derivatives
469. Analytical Estimation of Active Constituents in Nutraceuticals
470. Study on Oxidative Stability of Lipid-Based Drugs
471. Synthesis of Triazole–Isoxazole Derivatives for Antimicrobial Use
472. Analytical Quantification of Preservatives in Injectable Formulations
473. Synthesis of Pyridine–Benzimidazole Derivatives
474. Study on the Influence of Ionic Liquids in Drug Solubilization
475. Analytical Method Development for Peptide Impurity Profiling
476. Synthesis of Quinazoline–Coumarin Derivatives
477. Analytical Estimation of Bioactive Markers in Polyherbal Formulations
478. Synthesis of Indole–Isoxazole Hybrids for Antioxidant Activity
479. Study on the Correlation Between Drug Lipophilicity and Binding Affinity
480. Analytical Characterization of Biodegradable Polymers in Drug Delivery
481. Synthesis of Thiazole–Benzimidazole–Pyrazole Hybrids
482. Analytical Determination of Drug–Metabolite Ratios in Plasma
483. Synthesis and Evaluation of Isoxazole–Quinoline Analogs
484. Study on the Role of Metal Ions in Drug Activation Mechanisms
485. Analytical Profiling of Stress-Degraded Drug Products
486. Synthesis of Benzothiazole–Oxadiazole Derivatives
487. Study on Solvent–Solute Interactions in Drug Crystallization
488. Analytical Determination of Impurities in Hormonal Formulations
489. Synthesis of Thiadiazole–Quinazoline Hybrids
490. Validation of Analytical Methods for Peptide Quantification
491. Synthesis and Characterization of Pyridine–Thiazole Analogs
492. Analytical Determination of Drugs Using HILIC Techniques
493. Study on the Relationship Between Chemical Reactivity and Toxicity
494. Synthesis of Fused Heterocyclic Quantum Dot Conjugates for Imaging
495. Analytical Profiling of Drug Degradation in Metaverse-Simulated Environments
496. Synthesis of Neural Network-Optimized Heterocycles for Targeted Therapy
497. Study on Blockchain-Verified Impurity Tracking in API Synthesis
498. Development of AI-Driven QSAR Models for Drug Discovery Acceleration
499. Synthesis of Plasma-Enhanced Nanostructures for Drug Delivery Systems
500. Analytical Validation of Wormhole-Accelerated Stability Testing Protocols
Available Projects By Universities
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