XRF
 
 
Supermini Application Byte

 

Drug development

New drug discoveries not only help secure the financial health of pharmaceutical companies, they are paramount to the management of disease and the furtherance of human health and wellness. In the synthesis of new compounds for drug efficacy studies, researchers may be impacted by experimental, budgetary or other constraints as to the quantity of suitably pure material that can be produced in the laboratory for subsequent evaluation. These sample size limitations complicate chemical characterization of the synthetic products since very little material can be sacrificed for analysis.

 

Supermini

 

Microcarry

Rigaku's patented Microcarry and Ultracarry filters offer a uniquely fast, convenient and cost-effective means of conducting reliable elemental analyses of minute quantities of these drug candidates. The high detection sensitivities achievable with this sample preparation method often permit analyses to be conducted on lower cost benchtop WDXRF models with reduced utility and maintenance requirements such as Rigaku's high performance 200 Watt Supermini WDXRF spectrometer.

The WDXRF calibration curve shown in Figure 1 was constructed by pipetting microgram quantities of 2-bromo-5-aminothiazole monohydrobromide (Sigma-Aldrich, 61.48 mass% Br theoretical) from a 1.00 mg/mL aqueous stock solution onto the center analysis region of Microcarry filters. Measurement of bromine x-ray emission intensity from duplicate preparations of these filters using the Supermini gave a correlation coefficient of 0.998 and accuracy (RMS deviation) of 0.8 micrograms when calibrating in a Br loading range of 0 - 31 micrograms.

Figure 1. WDXRF bromine calibration curve

Two "prediction samples" prepared in duplicate per Table 1 from samples of arecoline hydrobromide (Sigma-Aldrich, 33.84 mass% Br theor.) and tetrabutylammonium bromide (Sigma-Aldrich, 24.79 mass% Br theor.) were analyzed against the WDXRF calibration curve to determine bromine loadings for method validation purposes, the results of which are presented in Table 2. One of the Microcarry filters prepared from these samples was analyzed ten different times and yielded the repeatability statistics of Table 3.

Sample ID

Mass (mg) 

Volume of water (mL)

Conc. (mg/mL)

Volume added to Microcarry filter (μL)

Total mass added to Microcarry filter (mg)

Mass of Br added to Microcarry filter (mg)

HAL-B-105-2

5.253

5.00

1.051

50

0.0526

0.0178

HAL-0B-195-3

4.801

5.00

0.960

50

0.0480

0.0119

Table 1: Preparation of prediction samples. HAL-B-195-2 prepared from arecoline hydrobromide, C3H13NO2 · HBr (33.84 mass% Br). HAL-B-195-3 prepared from tetrabutylammonium bromide, C16H36BrN (24.79 mass% Br)

Sample ID

Mass of Br added to Microcarry filter (mg)

Mass of Br on filter per WDXRF analysis (mg)

HAL-B-195-2

0.0178

0.0189

HAL-B-195-2B
(duplicate preparation)

0.0178

0.0180

 

Average = 0.0184

HAL-B-195-3

0.0119

0.0126

HAL-B-195-2B
(duplicate preparation)

0.0119

0.0113

  

Average = 0.0120

Table 2: Results for prediction samples

 

Run No.

Br (mg)

1

0.0182

2

0.0179

3

0.0179

4

0.0182

5

0.0182

6

0.0178

7

0.0180

8

0.0182

9

0.0180

10

0.0181

Mean

0.0180

Minimum

0.0178

Maximum

0.0182

Range

0.0004

Std. Dev

0.00015

RSD (%)

0.85

Table 3: Repeatability statistics

Coupled with the Supermini, the Microcarry method affords a bromine detection limit of 0.2 micrograms (Table 4) when using a 60 second counting time at peak and background locations. Analysis of the two prediction samples demonstrates the high accuracy potential of the method and its applicability to bromine compounds of widely differing chemical composition. Relative measurement errors of just 3.4% and 0.84% were indicated for arecoline hydrobromide and tetrabutylammonium bromide, respectively, when comparing WDXRF results to the theoretical Br content of the two materials. Replicate analyses of the former sample indicate bromine measurements can be made with high precision as evidenced by a 0.85% RSD.

Term

Value

m

33892

Rb

358

Tb

60

LLD (mg)

0.00022

Table 4. Bromine lower limit of detection. 

Formula: Lower limit of detection (LLD) in mg = 3/m x √(Rb-tb), where

  • m = sensitivity in counts/second per mg

  • Rb = count rate at background in counts/sec

  • tb = time at background in seconds

 

Tags: XRF, Supermini, high-power WDXRF, drug discovery, bromine, microcarry, pharmaceuticals